Search Ontology:
Human Disease

hereditary night blindness

Term ID
DOID:8498
Synonyms
  • Congenital night blindness
Definition
References
  • ICD10CM:H53.63
  • ICD9CM:368.61
  • MESH:C537743
  • SNOMEDCT_US_2023_03_01:193687000
  • UMLS_CUI:C1306122
Ontology
Human Disease   ( DOID:8498 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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