Search Ontology:
Human Disease
Mast syndrome
- Term ID
- DOID:0060245
- Synonyms
-
- autosomal recessive spastic paraplegia 21
- autosomal recessive spastic paraplegia type 21
- hereditary spastic paraplegia 21
- SPG21
- Definition
- A hereditary spastic paraplegia associated with dementia. (2)
- References
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- ICD10CM:G11.4
- MESH:C565409
- OMIM:248900
- ORDO:101001
- Ontology
- Human Disease ( DOID:0060245 )
- is a type of
-
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