DNHD1

dynein heavy chain domain 1
OMIM: 617277, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red DNHD1 in Rare multisystem ciliopathy disorders

Level 3: Congenital malformations caused by ciliopathies
Level 2: Ciliopathies
Version 1.170

review Not set
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • No OMIM phenotype