Pelizaeus-Merzbacher-like disease, autosomal recessive, 2

Preferred Label : Pelizaeus-Merzbacher-like disease, autosomal recessive, 2;

MeSH synonym : perinatal sudanophilic leukodystrophy; leukodystrophy, hypomyelinating, 3;

Details

Origin ID

C536319;

UMLS CUI

C1850053;

Currated CISMeF NLP mapping
- Leukodystrophy, hypomyelinating, 3 [OMIM Phenotype]
- Pelizaeus-Merzbacher-like disease due to AIMP1 mutation [ORDO Disease]
- hypomyelinating leukodystrophy 3 [DO Concept]
MeSH term(s) associated for indexing
- diffuse cerebral sclerosis of schilder [MeSH Descriptor]
Record concept(s)
- Pelizaeus-Merzbacher-like disease, autosomal recessive, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Leukodystrophy, hypomyelinating, 3 [OMIM Phenotype]
- Pelizaeus-Merzbacher-like disease due to AIMP1 mutation [ORDO Disease]
- hypomyelinating leukodystrophy 3 [DO Concept]

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