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DO Term : hereditary spastic paraplegia 13 [DOID:0110766] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33.

synonyms:
OMIM:605280,
ORDO:100994,
GARD:9616,
autosomal dominant spastic paraplegia 13,
ICD10CM:G11.4,
605280,
SPG13

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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