RET

Panel	Reviews	Mode of inheritance	Details
Filter panels 23 panels
Green RET in Vasculitis Level 2: Immunological disorders Version 0.82	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RET in Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic Level 2: Renal and urinary tract disorders Version 0.117 Component of the following Super Panels: Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel Kidneyome_SuperPanel	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red RET in Cataract Level 2: Ophthalmological disorders Version 0.366	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services
Red RET in Central Hypoventilation Level 2: Neurology and neurodevelopmental disorders Version 1.5	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 0.25	review	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	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 0.301	review	Unknown	Sources Expert Review Green Melbourne Genomics Health Alliance Victorian Clinical Genetics Services Expert Review Green
Red RET in Interstitial Lung Disease Level 2: Respiratory disorders Version 1.0	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 Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RET in Calcium and Phosphate disorders Level 2: Renal and urinary tract disorders; Endocrine disorders Version 1.24	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Expert Review Green Expert Review Phenotypes Multiple endocrine neoplasia IIA, MIM# 171400 Multiple endocrine neoplasia IIB, MIM# 162300
Green RET in Additional findings_Adult Level 2: Screening Version 0.166	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 0.6063	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
Red RET in CGC_86 Version 0.2	review	Other	Sources CGC_86 Phenotypes Multiple endocrine neoplasia, type 2b Multiple endocrine neoplasia, type 2a Familial medullary thyroid carcinoma
Red RET in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Multiple endocrine neoplasia, type 2b Multiple endocrine neoplasia, type 2a Familial medullary thyroid carcinoma
Red RET in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Familial medullary thyroid carcinoma Multiple endocrine neoplasia, type 2b Multiple endocrine neoplasia, type 2a
Green RET in Gastrointestinal neuromuscular disease Level 2: Gastroenterological disorders Version 1.24 Component of the following Super Panels: Neuromuscular Superpanel	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 0.278	review	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	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green RET in Fetal anomalies Version 1.255	review	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 BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category A gene Phenotypes Multiple endocrine neoplasia IIA Multiple endocrine neoplasia IIB Tags cancer treatable
Green RET in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.14 Component of the following Super Panels: Kidneyome_SuperPanel	review	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 1.0	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 Superpanel Level 2: Screening Version 0.18	review	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

RET

23 panels

Green RET in Vasculitis

Sources

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

Sources

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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Red RET in Interstitial Lung Disease

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Phenotypes

Green RET in Cancer Predisposition_Paediatric

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Green RET in Calcium and Phosphate disorders

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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

Red RET in CGC_86

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Phenotypes

Red RET in NCGC

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Phenotypes

Red RET in TCGA_PANCAN_2018

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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 BabyScreen+ newborn screening

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Phenotypes

Tags

Green RET in Renal Tubulopathies and related disorders

Sources

Phenotypes

Green RET in Facial papules

Sources

Phenotypes

Green RET in Transplant Co-Morbidity Superpanel

Sources

Phenotypes