FAM136A

family with sequence similarity 136 member A
OMIM: 616275, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber FAM136A in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.1

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
  • Other
Phenotypes
  • Meniere disease
Tags
  • watchlist
  • multifactorial