FAM177A1:Ensemblv90

family with sequence similarity 177 member A1
ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green FAM177A1 in Mendeliome


Version 1.3802

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with white matter abnormalities and gait disturbance, MIM# 621152

Green FAM177A1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.508

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with white matter abnormalities and gait disturbance, MIM# 621152

Green FAM177A1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Neurodevelopmental disorder with white matter abnormalities and gait disturbance, MIM# 621152