CFAP44

cilia and flagella associated protein 44
OMIM: 617559, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CFAP44 in Rare multisystem ciliopathy disorders

Level 3: Congenital malformations caused by ciliopathies
Level 2: Ciliopathies
Version 1.172

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • ?Spermatogenic failure 20 617593