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DO Term : hereditary spastic paraplegia 2 [DOID:0110773] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.

synonyms:
OMIM:312920,
spastic paraplegia type 2,
ORDO:99015,
X-linked spastic paraplegia 2,
ICD10CM:G11.4,
312920,
SPG2,
GARD:4923

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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