FAM177A1

family with sequence similarity 177 member A1
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green FAM177A1 in Mendeliome


Version 1.2655

review 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 1.174

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