Search Ontology:
Human Disease

hereditary retinal dystrophy

Term ID
DOID:8500
Synonyms
Definition
References
  • ICD10CM:H35.5
  • ICD9CM:362.7
  • NCI:C35194
  • SNOMEDCT_US_2023_03_01:41799005
  • UMLS_CUI:C0154860
Ontology
Human Disease   ( DOID:8500 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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