RET

Panel	Reviews	Mode of inheritance	Details
Filter panels 22 panels
Green RET in Congenital anomalies of the kidney and urinary tract (CAKUT) Level 2: Renal and urinary tract disorders Version 0.201 Component of the following Super Panels: Kidneyome_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Expert Review Green Victorian Clinical Genetics Services Phenotypes CAKUT MONDO:0019719, RET-related
Red RET in Cataract Level 2: Ophthalmological disorders Version 0.631	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services
Red RET in Central Hypoventilation Level 2: Neurology and neurodevelopmental disorders Version 1.7	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM#209880
Green RET in Hirschsprung disease Level 2: Gastroenterological disorders Version 0.28	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Multiple endocrine neoplasia IIA, MIM# 171400 Hirschsprung disease
Green RET in Hypercalcaemia Level 2: Endocrine disorders Version 1.2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Multiple endocrine neoplasia IIA, MIM# 171400 Multiple endocrine neoplasia IIB, MIM# 162300
Green RET in Incidentalome Version 0.430	1 review	Unknown	Sources Expert Review Green Melbourne Genomics Health Alliance Victorian Clinical Genetics Services Expert Review Green
Green RET in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.133	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red RET in Pulmonary Fibrosis_Interstitial Lung Disease Level 2: Respiratory disorders Version 1.9	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM#209880
Green RET in Additional findings_Adult Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Multiple endocrine neoplasia IIA, MIM# 171400 Multiple endocrine neoplasia IIB, MIM# 162300
Red RET in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.699	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genetic Health Queensland Phenotypes Central hypoventilation syndrome, congenital, MIM#209880 Medullary thyroid carcinoma, MIM#155240 Multiple endocrine neoplasia IIA, MIM#171400 Multiple endocrine neoplasia IIB, MIM#162300
Green RET in Gastrointestinal neuromuscular disease Level 2: Gastroenterological disorders Version 1.25 Component of the following Super Panels: Neuromuscular Superpanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Central hypoventilation syndrome, congenital, MIM# 209880 Multiple endocrine neoplasia IIA, MIM# 171400 Multiple endocrine neoplasia IIB, MIM# 162300
Green RET in Additional findings_Paediatric Level 2: Screening Version 0.280	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Multiple endocrine neoplasia IIA Multiple endocrine neoplasia IIB
Green RET in Incidentalome_PREGEN_DRAFT Version 0.43	0 reviews	Unknown	Sources NSW Health Pathology Expert Review Green
Green RET in Fetal anomalies Version 1.542	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Central hypoventilation syndrome, congenital, MIM#209880 Multiple endocrine neoplasia IIA, MIM#171400 Multiple endocrine neoplasia IIB, MIM#162300
Green RET in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.147	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category A gene Phenotypes Multiple endocrine neoplasia IIB Multiple endocrine neoplasia IIA Tags cancer treatable
Green RET in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.25 Component of the following Super Panels: Kidneyome_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Expert Review Green Expert list Expert Review Green Expert Review Phenotypes Multiple endocrine neoplasia IIB, MIM# 162300 Multiple endocrine neoplasia IIA, MIM# 171400
Green RET in Facial papules Level 2: Dermatological disorders Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes multiple endocrine neoplasia type 2B MONDO:0008082
Green RET in Transplant Co-Morbidity Level 2: Screening Version 0.21	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Multiple endocrine neoplasia IIB, MIM# 162300 Multiple endocrine neoplasia IIA, MIM# 171400
Green RET in Thyroid Cancer Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Thyroid cancer, MONDO:0002108 Medullary thyroid gland carcinoma, MONDO:0015277 Multiple endocrine neoplasia type 2A, MONDO:0008234 Multiple endocrine neoplasia type 2B, MONDO:0008082 Multiple endocrine neoplasia, type 2A, MIM#171400 Multiple endocrine neoplasia, type 2B, MIM#162300 Pheochromocytoma, MIM#171300 Medullary thyroid carcinoma, MIM#155240 Pheochromocytoma, susceptibility to, MIM#171300
Green RET in Parathyroid Tumour Level 2: Cancer Predisposition Version 1.2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Tumor of parathyroid gland, MONDO:0021360 Multiple endocrine neoplasia type 2A, MONDO:0008234 Multiple endocrine neoplasia type 2B, MONDO:0008082 Multiple endocrine neoplasia, type 2A, MIM#171400 Multiple endocrine neoplasia, type 2B, MIM#162300 Pheochromocytoma, MIM#171300 Medullary thyroid carcinoma, MIM#155240 Pheochromocytoma, susceptibility to, MIM#171300
Green RET in Paraganglioma_phaeochromocytoma Level 2: Cancer Predisposition Version 1.2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Paraganglioma, MONDO:0000448 Pheochromocytoma, MONDO:0008233 Multiple endocrine neoplasia type 2A, MONDO:0008234 Multiple endocrine neoplasia type 2B, MONDO:0008082 Multiple endocrine neoplasia, type 2A, MIM#171400 Multiple endocrine neoplasia, type 2B, MIM#162300 Pheochromocytoma, MIM#171300 Medullary thyroid carcinoma, MIM#155240 Pheochromocytoma, susceptibility to, MIM#171300
Green RET in Hyperparathyroidism Level 3: Calcium disorders Level 2: Endocrine disorders Version 0.12	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Expert list Expert Review Phenotypes Multiple endocrine neoplasia IIA, MIM# 171400 Multiple endocrine neoplasia IIB, MIM# 162300

RET

22 panels

Green RET in Congenital anomalies of the kidney and urinary tract (CAKUT)

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Phenotypes

Red RET in Cataract

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Red RET in Central Hypoventilation

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Phenotypes

Green RET in Hirschsprung disease

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Phenotypes

Green RET in Hypercalcaemia

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Phenotypes

Green RET in Incidentalome

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Green RET in Cancer Predisposition_Paediatric

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Red RET in Pulmonary Fibrosis_Interstitial Lung Disease

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Phenotypes

Green RET in Additional findings_Adult

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Phenotypes

Red RET in Intellectual disability syndromic and non-syndromic

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Phenotypes

Green RET in Gastrointestinal neuromuscular disease

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Phenotypes

Green RET in Additional findings_Paediatric

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Phenotypes

Green RET in Incidentalome_PREGEN_DRAFT

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Green RET in Fetal anomalies

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Phenotypes

Green RET in Genomic newborn screening: BabyScreen+

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Phenotypes

Tags

Green RET in Renal Tubulopathies and related disorders

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Phenotypes

Green RET in Facial papules

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Phenotypes

Green RET in Transplant Co-Morbidity

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Phenotypes

Green RET in Thyroid Cancer

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Phenotypes

Green RET in Parathyroid Tumour

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Phenotypes

Green RET in Paraganglioma_phaeochromocytoma

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Phenotypes

Green RET in Hyperparathyroidism

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Phenotypes