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DO Term : hereditary spastic paraplegia 6 [DOID:0110811] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.

synonyms:
autosomal dominant spastic paraplegia type 6,
OMIM:600363,
ICD10CM:G11.4,
autosomal dominant familial spastic paraplegia type 3,
600363,
FSP3,
ORDO:100988,
autosomal dominant spastic paraplegia 6,
SPG6

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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