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Huntington disease-like syndrome due to C9ORF72 expansions

Go to external page http://purl.obolibrary.org/obo/MONDO_0018425

Synonyms: C9ORF72-related Huntington disease-like syndrome Huntington disease phenocopy due to C9ORF72 expansions C9ORF72-related Huntington disease phenocopy

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1676144 (MONDO:equivalentTo)
  • UMLS:C5190586 (MONDO:equivalentTo)
  • Orphanet:401901 (MONDO:equivalentTo)
  • GARD:21702 (MONDO:GARD)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

exactMatch

http://www.orpha.net/ORDO/Orphanet_401901

http://identifiers.org/medgen/1676144

http://linkedlifedata.com/resource/umls/id/C5190586

id

MONDO:0018425