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DO Term : hereditary spastic paraplegia 3A [DOID:0110791] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.

synonyms:
autosomal dominant spastic paraplegia 3,
FSP1,
OMIM:182600,
ICD10CM:G11.4,
ORDO:100984,
autosomal dominant spastic paraplegia type 3,
GARD:5041,
autosomal dominant familial spastic paraplegia 1,
strumpell disease,
182600,
SPG3A

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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