Search Ontology:
Human Disease

neuronal ceroid lipofuscinosis

Term ID
DOID:14503
Synonyms
  • hereditary ceroid lipofuscinosis
Definition
References
  • GARD:10739
  • ICD10CM:E75.4
  • MESH:D009472
  • MIM:PS256730
  • NCI:C61257
  • ORDO:216
  • ORDO:79262
  • SNOMEDCT_US_2023_03_01:42012007
  • UMLS_CUI:C0027877
Ontology
Human Disease   ( DOID:14503 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models