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