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DO Term : hereditary spastic paraplegia 29 [DOID:0110780] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1.

synonyms:
ICD10CM:G11.4,
609727,
autosomal dominant spastic paraplegia 29,
SPG29,
ORDO:101009,
OMIM:609727,
GARD:9729

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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