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DO Term : hereditary spastic paraplegia 90A [DOID:0070459] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in heterozygous mutation in the SPTSSA gene on chromosome 14q13.1.

synonyms:
SPG90A,
620416,
OMIM:620416,
autosomal dominant spastic paraplegia 90A

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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