ADGRV1

adhesion G protein-coupled receptor V1
OMIM: 602851
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hearing loss, Febrile seizures, familial, 4, 604352, Syndromic and Non Syndromic Hearing Loss, Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472, Usher syndrome, type 2C, 605472
R-numbers: R32
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Usher syndrome, type 2C, 605472, Eye Disorders, Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472