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Huntington disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0007739

Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia. [ Orphanet:399 ]

Synonyms: Huntington's chorea Huntington's Disease Huntington disease Huntington chorea HD Huntington's disease

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:143100 (Orphanet:399/e)
  • GARD:6677 (MONDO:GARD)
  • ICD9:333.4 (MONDO:i2s)
  • Orphanet:399 (OMIM:143100)
  • NANDO:1200012 (https://orcid.org/0000-0003-0011-764X)
  • NORD:1256 (MONDO:NORD)
  • MESH:D006816 (https://orcid.org/0000-0003-1967-3726)
  • SCTID:58756001 (MONDO:equivalentTo)
  • UMLS:C0020179 (MONDO:equivalentTo)
  • icd11.foundation:2132180242 (Orphanet:399)
  • NCIT:C82342 (MONDO:equivalentTo)
  • MEDGEN:5654 (MONDO:equivalentTo)
  • DOID:12858 (MONDO:equivalentTo)
  • MedDRA:10070668 (Orphanet:399/e)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare, clingen

closeMatch

http://identifiers.org/meddra/10070668

exactMatch

http://www.orpha.net/ORDO/Orphanet_399

http://identifiers.org/snomedct/58756001

http://purl.obolibrary.org/obo/DOID_12858

https://omim.org/entry/143100

http://identifiers.org/medgen/5654

http://purl.obolibrary.org/obo/NCIT_C82342

http://linkedlifedata.com/resource/umls/id/C0020179

http://identifiers.org/mesh/D006816

id

MONDO:0007739