Synonyms: PCH13 PONTOCEREBELLAR HYPOPLASIA, TYPE 13

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:18031 (MONDO:GARD)
  • UMLS:C5231425 (MONDO:equivalentTo)
  • DOID:0112332 (MONDO:equivalentTo)
  • Orphanet:613267 (MONDO:equivalentTo)
  • OMIM:618606 (MONDO:equivalentTo)
  • MEDGEN:1684708 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disorder, rare, nord_rare, orphanet_rare

exactMatch

http://www.orpha.net/ORDO/Orphanet_613267

http://purl.obolibrary.org/obo/DOID_0112332

https://omim.org/entry/618606

http://identifiers.org/medgen/1684708

http://linkedlifedata.com/resource/umls/id/C5231425

id

MONDO:0032831

Term relations