HNF4A

hepatocyte nuclear factor 4 alpha
OMIM: 600281, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green HNF4A in Hyperinsulinism Level 2: Endocrine disorders Version 1.30	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, OMIM #616026 MODY, type I, OMIM # 125850
Green HNF4A in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, OMIM #616026 MODY, type I, OMIM # 125850
Green HNF4A in Maturity-onset Diabetes of the Young Level 2: Endocrine disorders Version 1.21	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Royal Melbourne Hospital Victorian Clinical Genetics Services Phenotypes Maturity Onset Diabetes of the Young MODY, type I, 125850 OMIM 616026
Green HNF4A in Monogenic Diabetes Level 2: Endocrine disorders Version 0.136 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young 616026 Maturity-Onset Diabetes Of The Young, Type 1 MODY1, 125850 {Diabetes mellitus, noninsulin-dependent}, 125853
Green HNF4A in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category C gene Phenotypes Hypoglycaemia, hyperinsulinaemic
Green HNF4A in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young MIM#616026
Amber HNF4A in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category C gene BeginNGS Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, MIM# 616026 Hypoglycaemia, hyperinsulinaemic, MIM#125850 MODY, type I, OMIM # 125850 Tags for review endocrine
Green HNF4A in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.17 Component of the following Super Panels: Kidneyome_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green KidGen_Tubulopathies v38.1.0 Phenotypes MODY, type I, OMIM # 125850 Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, OMIM #616026
Green HNF4A in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young 616026 MODY1, 125850 {Diabetes mellitus, noninsulin-dependent}, 125853 Maturity-Onset Diabetes Of The Young, Type 1