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inherited retinal dystrophy

Disease Summary
Associated Targets (626)
Tbio

449

Tchem

93

Tclin

49

Tdark

35


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: