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inherited retinal dystrophy

Disease Summary
Associated Targets (601)
Tbio

431

Tchem

89

Tclin

47

Tdark

34


Explore Associated Targets
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: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
Tbio

476

Tchem

108

Tclin

81

Tdark

36

Tbio

470

Tchem

93

Tclin

47

Tdark

34

Tbio

435

Tchem

92

Tclin

48

Tdark

34

Children
Tbio

234

Tchem

37

Tclin

35

Tdark

6

Tbio

150

Tchem

38

Tdark

24

Tclin

12

Tbio

158

Tchem

22

Tclin

9

Tdark

7

Target Novelty (Tin-x)