spastic paraplegia 33, autosomal dominant

Preferred Label : spastic paraplegia 33, autosomal dominant;

MeSH note : also known as SPG33; associated with mutations in ZFYVE27, the gene for zinc finger FYVE domain-containing protein 27;

Détails

Origin ID

C565214;

UMLS CUI

C1853251;

Automatic exact mappings (from CISMeF team)
- hereditary spastic paraplegia 33 [DO Concept]
Currated CISMeF NLP mapping
- Spastic paraplegia 33, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia 33, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic paraplegia 33, autosomal dominant [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

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