You are using an outdated browser. Please upgrade your browser to improve your experience.

retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal dominant retinal dystrophy characterized by inner retinal dysfunction in association with ganglion cell abnormalities. Clinical features include mild photophobia, progressive loss of central vision, night blindness, and hyperreflectivity of nerve and ganglion cell layers.
Mondo Term and Equivalent IDs
MONDO:0014483:  retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
Orphanet:397758: 
UMLS:C4015146: