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{
"count": 221277,
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"results": [
{
"created": "2020-08-27T21:00:31.751109+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fumarase deficiency for gene: FH",
"entity_name": "FH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:31.455826+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Afibrinogenaemia for gene: FGG",
"entity_name": "FGG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:30.938656+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Muenke syndrome for gene: FGFR3",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:30.641558+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Thanatophoric dysplasia type 1 for gene: FGFR3",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:30.339505+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Crouzon syndrome with acanthosis nigricans for gene: FGFR3",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:30.062927+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hypochondroplasia for gene: FGFR3",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:29.738421+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Achondroplasia for gene: FGFR3",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:29.439208+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Jackson-Weiss syndrome for gene: FGFR2",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:29.140055+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Beare-Stevenson cutis gyrata syndrome for gene: FGFR2",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:28.844107+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Crouzon syndrome for gene: FGFR2",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:28.331126+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Apert syndrome for gene: FGFR2",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:28.038178+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Pfeiffer syndrome for gene: FGFR2",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:27.731792+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Kallmann syndrome for gene: FGFR1",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:27.437675+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Deafness, congenital with inner ear agenesis, microtia, and microdontia for gene: FGF3",
"entity_name": "FGF3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:27.142388+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: FGD4",
"entity_name": "FGD4",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:26.842394+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Aarskog-Scott syndrome for gene: FGD1",
"entity_name": "FGD1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:26.542196+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Afibrinogenaemia for gene: FGB",
"entity_name": "FGB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:26.246136+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Afibrinogenaemia for gene: FGA",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:25.736083+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Contractural arachnodactyly for gene: FBN2",
"entity_name": "FBN2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:25.438554+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Marfan's syndrome for gene: FBN1",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:25.138793+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Cutis laxa for gene: FBLN5",
"entity_name": "FBLN5",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:24.842186+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCI",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:24.542538+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCG",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:24.251427+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCD2",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:24.018811+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCC",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:23.650374+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCB",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:23.418656+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Fanconi anaemia for gene: FANCA",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:23.124601+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Syndactyly - telecanthus - anogenital and renal malformations for gene: FAM58A",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:22.541251+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Osteosclerotic bone dysplasia for gene: FAM20C",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:22.247789+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Retinal dystrophy for gene: FAM161A",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:21.950848+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hypomyelination and congenital cataract for gene: FAM126A",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:21.718706+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Tyrosinemia, type I for gene: FAH",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:21.425103+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hemophilia B for gene: F9",
"entity_name": "F9",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:21.126180+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hemophilia A for gene: F8",
"entity_name": "F8",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:20.830442+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Prothrombin deficiency for gene: F2",
"entity_name": "F2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:20.536153+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Factor XI deficiency for gene: F11",
"entity_name": "F11",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:20.235149+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Weaver syndrome 2 for gene: EZH2",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:19.936867+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Deafness, autosomal dominant for gene: EYA4",
"entity_name": "EYA4",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:19.426015+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Branchiootorenal syndrome for gene: EYA1",
"entity_name": "EYA1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:19.131280+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Exostoses, multiple, type 2 for gene: EXT2",
"entity_name": "EXT2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:18.835205+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Exostoses, multiple, type 1 for gene: EXT1",
"entity_name": "EXT1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:18.539099+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ellis-van Creveld syndrome for gene: EVC2",
"entity_name": "EVC2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:18.244511+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ellis-van Creveld syndrome for gene: EVC",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:17.947044+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ethylmalonic encephalopathy for gene: ETHE1",
"entity_name": "ETHE1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:17.642096+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glutaric acidemia IIC for gene: ETFDH",
"entity_name": "ETFDH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:17.349463+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glutaric acidemia IIB for gene: ETFB",
"entity_name": "ETFB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:16.837882+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Glutaric acidemia IIA for gene: ETFA",
"entity_name": "ETFA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:16.541341+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: ESRRB",
"entity_name": "ESRRB",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:16.245486+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Roberts syndrome for gene: ESCO2",
"entity_name": "ESCO2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:15.950220+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Cockayne syndrome for gene: ERCC8",
"entity_name": "ERCC8",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:15.696804+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Cockayne syndrome for gene: ERCC6",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:15.354129+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Xeroderma pigmentosum for gene: ERCC5",
"entity_name": "ERCC5",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:15.117456+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Xeroderma pigmentosum for gene: ERCC2",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:14.819657+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Epilepsy, progressive myoclonic 2A (Lafora) for gene: EPM2A",
"entity_name": "EPM2A",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:14.523398+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Arterial calcification, generalized, of infancy, 1 for gene: ENPP1",
"entity_name": "ENPP1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:13.961521+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Telangiectasia, hereditary hemorrhagic, type 1 for gene: ENG",
"entity_name": "ENG",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:13.642483+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, Emery-Dreifuss for gene: EMD",
"entity_name": "EMD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:13.350194+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Supravalvar aortic stenosis for gene: ELN",
"entity_name": "ELN",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:13.062775+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Neutropenia, congenital for gene: ELANE",
"entity_name": "ELANE",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:12.818779+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Wolcott-Rallison syndrome for gene: EIF2AK3",
"entity_name": "EIF2AK3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:12.526222+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: EGR2",
"entity_name": "EGR2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:12.235704+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mandibulofacial dysostosis with microcephaly for gene: EFTUD2",
"entity_name": "EFTUD2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:11.935010+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Myoclonic epilepsy for gene: EFHC1",
"entity_name": "EFHC1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:11.628957+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDARADD",
"entity_name": "EDARADD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:11.057215+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDAR",
"entity_name": "EDAR",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:10.752216+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDA",
"entity_name": "EDA",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:10.454725+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Miyoshi muscular dystrophy 1 for gene: DYSF",
"entity_name": "DYSF",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:10.218726+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, type 2B for gene: DYSF",
"entity_name": "DYSF",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:09.918718+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Thyroid dyshormonogenesis for gene: DUOX2",
"entity_name": "DUOX2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:09.626143+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Epidermolysis bullosa, lethal acantholytic for gene: DSP",
"entity_name": "DSP",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:09.331014+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 disorder of glycosylation, type Ij for gene: DPAGT1",
"entity_name": "DPAGT1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:09.048170+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 for gene: DOK7",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:08.732935+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hyper-IgE syndrome for gene: DOCK8",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:08.436017+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Immunodeficiency-centromeric instability-facial anomalies syndrome 1 for gene: DNMT3B",
"entity_name": "DNMT3B",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:07.850377+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, axonal, type 2M for gene: DNM2",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:07.549089+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Myopathy, centronuclear for gene: DNM2",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:07.243870+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 for gene: DNAJB6",
"entity_name": "DNAJB6",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:06.953682+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Primary ciliary dyskinesia for gene: DNAI1",
"entity_name": "DNAI1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:06.648019+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Primary ciliary dyskinesia for gene: DNAH5",
"entity_name": "DNAH5",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:06.406598+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Primary ciliary dyskinesia for gene: DNAH11",
"entity_name": "DNAH11",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:06.046527+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Primary ciliary dyskinesia for gene: DNAAF1",
"entity_name": "DNAAF1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:05.743465+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Myotonic dystrophy 1 for gene: DMPK",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:05.224812+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Hypophosphatemic rickets, AR for gene: DMP1",
"entity_name": "DMP1",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:04.926756+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Becker muscular dystrophy for gene: DMD",
"entity_name": "DMD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:04.626257+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Duchenne muscular dystrophy for gene: DMD",
"entity_name": "DMD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:04.328442+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Spondylocostal dysostosis, autosomal recessive, 1 for gene: DLL3",
"entity_name": "DLL3",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:04.017461+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Maple syrup urine disease, type III for gene: DLD",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:03.649469+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Smith-Lemli-Opitz syndrome for gene: DHCR7",
"entity_name": "DHCR7",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:03.348332+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Mitochondrial DNA depletion syndrome for gene: DGUOK",
"entity_name": "DGUOK",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:03.053424+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: DFNB59",
"entity_name": "DFNB59",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:02.749657+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: DFNA5",
"entity_name": "DFNA5",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:02.228743+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Myopathy, myofibrillar for gene: DES",
"entity_name": "DES",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:01.930299+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Aromatic L-amino acid decarboxylase deficiency for gene: DDC",
"entity_name": "DDC",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:01.628181+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Xeroderma pigmentosum for gene: DDB2",
"entity_name": "DDB2",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:01.330815+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Lissencephaly, X-linked for gene: DCX",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:01.035195+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Severe combined immunodeficiency, Athabascan type for gene: DCLRE1C",
"entity_name": "DCLRE1C",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:00.736648+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Maple syrup urine disease for gene: DBT",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:00.433354+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes D-2-hydroxyglutaric aciduria for gene: D2HGDH",
"entity_name": "D2HGDH",
"entity_type": "gene"
},
{
"created": "2020-08-27T21:00:00.174097+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Ichthyosis, congenital, autosomal recessive for gene: CYP4F22",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2020-08-27T20:59:59.745490+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added phenotypes Vitamin D-dependent rickets, type I for gene: CYP27B1",
"entity_name": "CYP27B1",
"entity_type": "gene"
}
]
}