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DO Term : Mast syndrome [DOID:0060245] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia associated with dementia.
  • synonyms:
  • 248900,
  • SPG21,
  • ORDO:101001,
  • ICD10CM:G11.4,
  • hereditary spastic paraplegia 21,
  • autosomal recessive spastic paraplegia 21,
  • OMIM:248900,
  • MESH:C565409,
  • autosomal recessive spastic paraplegia type 21
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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