MAST syndrome - CISMeF

Preferred Label : MAST syndrome;

MeSH note : mutation in ACP33;

MeSH synonym : spastic paraplegia 21, autosomal recessive;

Origin ID

C565409;

UMLS CUI

C1855346;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 21 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 21 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 21 (disorder) [SNOMED CT concept]
- Mast syndrome [DO Concept]
- Mast syndrome [OMIM Phenotype]
DO Cross reference
- Mast syndrome [DO Concept]
MeSH term(s) associated for indexing
- dementia [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- MAST syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 21 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 21 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 21 (disorder) [SNOMED CT concept]
- Mast syndrome [OMIM Phenotype]
- Mast syndrome [DO Concept]