Synonyms: Huntington disease phenocopy syndrome
This is just here as a test because I lose it
Term information
database
cross reference
- SCTID:702376003 (MONDO:equivalentTo)
- ICD9:333.99 (MONDO:relatedTo)
- Orphanet:158266 (MONDO:equivalentTo)
- MESH:C580174 (MONDO:equivalentTo)
- UMLS:C3711380 (MONDO:equivalentTo)
- MEDGEN:777988 (MONDO:equivalentTo)
- GARD:20029 (MONDO:GARD)
Subsets
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
exactMatch
http://linkedlifedata.com/resource/umls/id/C3711380
http://identifiers.org/mesh/C580174
http://identifiers.org/snomedct/702376003
http://identifiers.org/medgen/777988
http://www.orpha.net/ORDO/Orphanet_158266