Synonyms: pontocerebellar hypoplasia, type 14 PCH14

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:18032 (MONDO:GARD)
  • OMIM:619301 (MONDO:equivalentTo)
  • UMLS:C5543322 (MONDO:equivalentTo)
  • DOID:0112325 (MONDO:equivalentTo)
  • MEDGEN:1778516 (MONDO:equivalentTo)
  • Orphanet:613274 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, rare, nord_rare, orphanet_rare

exactMatch

http://linkedlifedata.com/resource/umls/id/C5543322

http://identifiers.org/medgen/1778516

http://www.orpha.net/ORDO/Orphanet_613274

http://purl.obolibrary.org/obo/DOID_0112325

https://omim.org/entry/619301

id

MONDO:0030258

Term relations