Synonyms: hereditary ceroid lipofuscinosis

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D009472
  • MIM:PS256730
  • ICD10CM:E75.4
  • UMLS_CUI:C0027877
  • SNOMEDCT_US_2023_03_01:42012007
  • NCI:C61257
  • ORDO:216
  • GARD:10739
  • ORDO:79262
Subsets

DO_FlyBase_slim, DO_rare_slim, NCIthesaurus

comment

Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS].

has obo namespace

disease_ontology

id

DOID:14503

Term relations

Subclass of: