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inherited retinal dystrophy

Disease Summary
Associated Targets (626)
Tbio

456

Tchem

91

Tclin

49

Tdark

30


Mondo Description An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0019118:  inherited retinal dystrophy
COHD:377270: 
COHD:380395: 
ICD10:H35.5: 
ICD9:362.70: 
MESH:D058499: 
NCIT:C35194: 
NCIT:C35625: 
Orphanet:71862: 
SCTID:314407005: 
SCTID:41799005: 
UMLS:C0154860: 
UMLS:C0854723: