OBO ID: DOID:0060245
Term Name: Mast syndrome Search Ontology:
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:
Ontology: Human Disease   ( DOID:0060245 )
Relationships
is a type of:
OTHER Mast syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPG21 Mast syndrome 248900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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