CYP17A1

cytochrome P450 family 17 subfamily A member 1
OMIM: 609300, Gene2Phenotype

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Green CYP17A1 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 1.8	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110 Tags treatable
Green CYP17A1 in Mendeliome Version 1.2374	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110 Tags treatable
Green CYP17A1 in Hypertension and Aldosterone disorders Level 2: Renal and urinary tract disorders; Endocrine disorders Version 1.15 Component of the following Super Panels: Kidneyome_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110
Green CYP17A1 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes 17,20-lyase deficiency, isolated, 202110 (3)
Green CYP17A1 in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.340	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes 17-alpha-hydroxylase, 17,20-lyase deficiency 202110 Tags treatable
Green CYP17A1 in Fetal anomalies Version 1.314	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110
Green CYP17A1 in Prepair 1000+ Level 2: Screening Version 1.1586	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency MIM#202110
Green CYP17A1 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BeginNGS Phenotypes 17,20-lyase deficiency, isolated , MIM#202110 Tags treatable endocrine
Green CYP17A1 in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.18 Component of the following Super Panels: Kidneyome_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Expert list Expert Review Green KidGen_MetabolicRenal v38.1.0 Expert Review Green Victorian Clinical Genetics Services Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110
Green CYP17A1 in Prepair 500+ Level 2: Screening Version 1.5	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes 17,20-lyase deficiency, isolated, 202110 (3)