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Pelizaeus-Merzbacher-like disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0017226

Pelizaeus-Merzbacher like disease (PMLD) is an autosomal recessive leukodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease (PMD). [ Orphanet:280270 ]

Synonyms: PMLD

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:894734 (MONDO:equivalentTo)
  • UMLS:C4274084 (MONDO:equivalentTo)
  • NANDO:2201289 (https://orcid.org/0000-0003-0011-764X)
  • SCTID:717042001 (MONDO:equivalentTo)
  • Orphanet:280270 (MONDO:equivalentTo)
  • NANDO:1200577 (https://orcid.org/0000-0003-0011-764X)
  • icd11.foundation:1101042369 (Orphanet:280270)
  • GARD:12300 (MONDO:GARD)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

exactMatch

http://linkedlifedata.com/resource/umls/id/C4274084

http://www.orpha.net/ORDO/Orphanet_280270

http://identifiers.org/snomedct/717042001

http://identifiers.org/medgen/894734

id

MONDO:0017226

seeAlso

https://rarediseases.info.nih.gov/diseases/12300/pelizaeus-merzbacher-like-disease

Term relations

Subclass of: