FAT1

FAT atypical cadherin 1
OMIM: 600976, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green FAT1 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.43	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes facial dysmorphism colobomatous microphthalmia ptosis syndactyly with or without nephropathy
Green FAT1 in Mendeliome Version 1.2302	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes syndromic disease MONDO:0002254, FAT1-related facial dysmorphism colobomatous microphthalmia ptosis syndactyly with or without nephropathy
Green FAT1 in Proteinuria Level 2: Renal and urinary tract disorders Version 0.229 Component of the following Super Panels: Kidneyome_SuperPanel Renal Glomerular Disease_SuperPanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes facial dysmorphism colobomatous microphthalmia ptosis syndactyly with or without nephropathy
Green FAT1 in Hand and foot malformations Level 2: Dysmorphic and congenital abnormality syndromes Version 0.76 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes facial dysmorphism colobomatous microphthalmia ptosis syndactyly with or without nephropathy
Green FAT1 in Fetal anomalies Version 1.313	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes multiple congenital anomalies nephropathy ocular anomalies hand and foot anomalies