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{
"count": 221277,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1645",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1643",
"results": [
{
"created": "2020-08-27T21:01:00.632727+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: INVS was added\ngene: INVS was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: INVS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: INVS were set to Nephronophthisis 2",
"entity_name": "INVS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:01:00.353513+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: INSR was added\ngene: INSR was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: INSR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: INSR were set to Leprechaunism",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:01:00.147838+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ILDR1 was added\ngene: ILDR1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: ILDR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ILDR1 were set to Deafness, autosomal recessive",
"entity_name": "ILDR1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:59.842555+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL2RG was added\ngene: IL2RG was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IL2RG was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: IL2RG were set to Severe combined immunodeficiency, X-linked",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:59.636836+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL10RA was added\ngene: IL10RA was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IL10RA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IL10RA were set to Inflammatory bowel disease",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:59.421047+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IKBKG was added\ngene: IKBKG was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IKBKG was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: IKBKG were set to Incontinentia pigmenti 1",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:59.146726+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ELP1 was added\ngene: ELP1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: ELP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ELP1 were set to Dysautonomia, familial",
"entity_name": "ELP1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:58.717473+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IGSF1 was added\ngene: IGSF1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IGSF1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: IGSF1 were set to Central hypothyroidism and testicular enlargement",
"entity_name": "IGSF1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:58.441484+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IGHMBP2 was added\ngene: IGHMBP2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IGHMBP2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IGHMBP2 were set to Spinal muscular atrophy with respiratory distress",
"entity_name": "IGHMBP2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:58.232514+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IDUA was added\ngene: IDUA was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IDUA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IDUA were set to Mucopolysaccharidosis Ih",
"entity_name": "IDUA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:57.951603+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IDS was added\ngene: IDS was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: IDS was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: IDS were set to Mucopolysaccharidosis II",
"entity_name": "IDS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:57.738636+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HTRA1 was added\ngene: HTRA1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HTRA1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HTRA1 were set to CARASIL syndrome",
"entity_name": "HTRA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:57.523923+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSPG2 was added\ngene: HSPG2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSPG2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HSPG2 were set to Schwartz-Jampel syndrome",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:57.244534+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSPB8 was added\ngene: HSPB8 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSPB8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HSPB8 were set to Charcot-Marie-Tooth disease, axonal, type 2L",
"entity_name": "HSPB8",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:57.041788+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSD3B7 was added\ngene: HSD3B7 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSD3B7 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HSD3B7 were set to 3 beta-hydroxysteroid dehydrogenase deficiency",
"entity_name": "HSD3B7",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:56.820823+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSD17B4 was added\ngene: HSD17B4 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSD17B4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HSD17B4 were set to D-bifunctional protein deficiency",
"entity_name": "HSD17B4",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:56.544227+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSD17B3 was added\ngene: HSD17B3 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSD17B3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HSD17B3 were set to Pseudohermaphroditism, male, with gynecomastia",
"entity_name": "HSD17B3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:56.334162+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSD17B10 was added\ngene: HSD17B10 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HSD17B10 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: HSD17B10 were set to 17-beta-hydroxysteroid dehydrogenase X deficiency",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:55.841470+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HRAS was added\ngene: HRAS was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HRAS were set to Costello syndrome",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:55.631155+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS5 was added\ngene: HPS5 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HPS5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HPS5 were set to Hermansky-Pudlak syndrome 5",
"entity_name": "HPS5",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:55.418720+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS4 was added\ngene: HPS4 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HPS4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HPS4 were set to Hermansky-Pudlak syndrome 4",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:55.150386+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS3 was added\ngene: HPS3 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HPS3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HPS3 were set to Hermansky-Pudlak syndrome 3",
"entity_name": "HPS3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:54.939697+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS1 was added\ngene: HPS1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HPS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HPS1 were set to Hermansky-Pudlak syndrome 1",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:54.733928+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPRT1 was added\ngene: HPRT1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HPRT1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: HPRT1 were set to Lesch-Nyhan syndrome 1",
"entity_name": "HPRT1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:54.523857+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HMGCL was added\ngene: HMGCL was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HMGCL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HMGCL were set to 3-hydroxy-3-methylglutaric aciduria",
"entity_name": "HMGCL",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:54.250459+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HLCS was added\ngene: HLCS was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HLCS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HLCS were set to Holocarboxylase synthetase deficiency",
"entity_name": "HLCS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:54.045987+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HINT1 was added\ngene: HINT1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HINT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HINT1 were set to Axonal neuropathy with neuromyotonia",
"entity_name": "HINT1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:53.829919+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HGSNAT was added\ngene: HGSNAT was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HGSNAT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HGSNAT were set to Mucopolysaccharidosis IIIC",
"entity_name": "HGSNAT",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:53.617447+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HGD was added\ngene: HGD was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HGD was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HGD were set to Alkaptonuria",
"entity_name": "HGD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:53.347478+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HEXB was added\ngene: HEXB was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HEXB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HEXB were set to Sandhoff disease, infantile, juvenile, and adult forms",
"entity_name": "HEXB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:53.140244+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HEXA was added\ngene: HEXA was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HEXA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HEXA were set to Tay-Sachs disease",
"entity_name": "HEXA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:52.933687+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HDAC8 was added\ngene: HDAC8 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HDAC8 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: HDAC8 were set to Cornelia de Lange syndrome-like features, ocular hypertelorism & large fontanelle",
"entity_name": "HDAC8",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:52.723412+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HBB was added\ngene: HBB was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HBB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HBB were set to Beta-thalassemia",
"entity_name": "HBB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:52.452023+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HBA2 was added\ngene: HBA2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HBA2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HBA2 were set to Thalassemia, alpha",
"entity_name": "HBA2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:52.030976+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HBA1 was added\ngene: HBA1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HBA1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HBA1 were set to Thalassaemia alpha",
"entity_name": "HBA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:51.821893+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HADHB was added\ngene: HADHB was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HADHB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HADHB were set to Mitochondrial trifunctional protein deficiency",
"entity_name": "HADHB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:51.547906+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HADHA was added\ngene: HADHA was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HADHA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HADHA were set to Mitochondrial trifunctional protein deficiency",
"entity_name": "HADHA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:51.338592+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HADH was added\ngene: HADH was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: HADH was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HADH were set to Hyperinsulinemic hypoglycemia, familial, 4",
"entity_name": "HADH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:51.135890+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: H19 was added\ngene: H19 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: H19 was set to Unknown\nPhenotypes for gene: H19 were set to Beckwith-Wiedemann Syndrome",
"entity_name": "H19",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:50.927246+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GYS2 was added\ngene: GYS2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: GYS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GYS2 were set to Glycogen storage disease 0",
"entity_name": "GYS2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:50.718720+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GUSB was added\ngene: GUSB was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: GUSB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GUSB were set to Mucopolysaccharidosis VII",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:50.451664+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GSS was added\ngene: GSS was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: GSS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GSS were set to Glutathione synthetase deficiency",
"entity_name": "GSS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:50.249199+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GRHPR was added\ngene: GRHPR was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: GRHPR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GRHPR were set to Hyperoxaluria, primary, type II",
"entity_name": "GRHPR",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:50.055480+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GPSM2 was added\ngene: GPSM2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene\nMode of inheritance for gene: GPSM2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GPSM2 were set to Chudley-McCullough syndrome",
"entity_name": "GPSM2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:49.746413+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Usher syndrome for gene: PDZD7",
"entity_name": "PDZD7",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:49.445590+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Polymicrogyria, bilateral frontoparietal for gene: ADGRG1",
"entity_name": "ADGRG1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:49.151034+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ocular albinism, type I for gene: GPR143",
"entity_name": "GPR143",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:48.635533+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Simpson-Golabi-Behmel syndrome for gene: GPC3",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:48.341528+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mucopolysaccharidosis IIId for gene: GNS",
"entity_name": "GNS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:48.044600+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mucolipidosis III gamma for gene: GNPTG",
"entity_name": "GNPTG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:47.750475+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mucolipidosis II for gene: GNPTAB",
"entity_name": "GNPTAB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:47.456873+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Inclusion body myopathy for gene: GNE",
"entity_name": "GNE",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:47.222844+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Pseudopseudohypoparathyroidism for gene: GNAS",
"entity_name": "GNAS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:46.926256+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Pseudohypoparathyroidism for gene: GNAS",
"entity_name": "GNAS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:46.624711+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hyperinsulinism for gene: GLUD1",
"entity_name": "GLUD1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:46.327863+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hyperekplexia, hereditary 1, autosomal dominant or recessive for gene: GLRA1",
"entity_name": "GLRA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:45.747013+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Greig cephalopolysyndactyly syndrome for gene: GLI3",
"entity_name": "GLI3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:45.451894+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glycine encephalopathy for gene: GLDC",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:45.161240+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Gangliosidosis GM1 for gene: GLB1",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:44.918698+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fabry disease for gene: GLA",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:44.621661+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Pelizaeus-Merzbacher-like disease for gene: GJC2",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:44.321628+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene GJB2 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nAdded phenotypes Deafness and palmoplantar keratoderma for gene: GJB2",
"entity_name": "GJB2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:44.024002+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene GJB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes Deafness for gene: GJB2",
"entity_name": "GJB2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:43.721716+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Charcot-Marie-Tooth neuropathy for gene: GJB1",
"entity_name": "GJB1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:43.427663+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Oculodentodigital dysplasia for gene: GJA1",
"entity_name": "GJA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:43.133521+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hearing loss for gene: GIPC3",
"entity_name": "GIPC3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:42.557630+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Congenital myasthenic syndrome, limb-girdle for gene: GFPT1",
"entity_name": "GFPT1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:42.318778+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Combined oxidative phosphorylation deficiency 1 for gene: GFM1",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:42.018954+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Alexander disease for gene: GFAP",
"entity_name": "GFAP",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:41.717447+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Charcot-Marie-Tooth disease for gene: GDAP1",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:41.352164+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hyperinsulinemic hypoglycemia, familial for gene: GCK",
"entity_name": "GCK",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:41.069142+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glutaricaciduria, type I for gene: GCDH",
"entity_name": "GCDH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:40.822032+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glycogen storage disease IV for gene: GBE1",
"entity_name": "GBE1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:40.523260+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Gaucher disease 1 for gene: GBA",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:39.947692+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Congenital heart defects for gene: GATA4",
"entity_name": "GATA4",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:39.645881+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Dyserythropoietic anemia with thrombocytopenia for gene: GATA1",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:39.345235+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Giant axonal neuropathy for gene: GAN",
"entity_name": "GAN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:39.050610+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Galactosaemia for gene: GALT",
"entity_name": "GALT",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:38.749275+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mucopolysaccharidosis IVA for gene: GALNS",
"entity_name": "GALNS",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:38.454637+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Galactokinase deficiency with cataracts for gene: GALK1",
"entity_name": "GALK1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:38.220739+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Krabbe disease for gene: GALC",
"entity_name": "GALC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:37.923442+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glycogen storage disease II for gene: GAA",
"entity_name": "GAA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:37.627936+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glucose-6-phosphate dehydrogenase deficiency for gene: G6PD",
"entity_name": "G6PD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:37.051278+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Neutropaenia, congenital for gene: G6PC3",
"entity_name": "G6PC3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:36.746666+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glycogen storage disease Ia for gene: G6PC",
"entity_name": "G6PC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:36.452502+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Friedreich ataxia for gene: FXN",
"entity_name": "FXN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:36.218704+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fucosidosis for gene: FUCA1",
"entity_name": "FUCA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:35.925444+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Neuroferritinopathy for gene: FTL",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:35.629215+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fraser syndrome for gene: FRAS1",
"entity_name": "FRAS1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:35.333245+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes IPEX syndrome for gene: FOXP3",
"entity_name": "FOXP3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:35.058325+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Alveolar capillary dysplasia with misalignment of pulmonary veins for gene: FOXF1",
"entity_name": "FOXF1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:34.728048+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Lymphoedema, primary for gene: FOXC2",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:34.147743+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Axenfeld-Rieger syndrome for gene: FOXC1",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:33.841185+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Otopalatodigital spectrum disorder for gene: FLNA",
"entity_name": "FLNA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:33.536759+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Birt-Hogg-Dube syndrome for gene: FLCN",
"entity_name": "FLCN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:33.239133+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies for gene: FKTN",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:32.940412+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Muscular dystrophy, Fukuyama for gene: FKTN",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:32.639072+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Muscle-eye-brain disease for gene: FKRP",
"entity_name": "FKRP",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:32.343807+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Muscular dystrophy, limb girdle 2I for gene: FKRP",
"entity_name": "FKRP",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:32.056669+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Emery-Dreifuss muscular dystrophy for gene: FHL1",
"entity_name": "FHL1",
"entity_type": "gene"
}
]
}