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DO Term : hereditary spastic paraplegia 17 [DOID:0110770] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.

synonyms:
distal hereditary motor neuropathy type 5B,
dHMN5B,
spastic paraplegia with amyotrophy of hands and feet,
270685,
GARD:4219,
OMIM:270685,
autosomal dominant spastic paraplegia 17,
ORDO:100998,
ICD10CM:G11.4,
SPG17,
Silver syndrome,
autosomal dominant spastic paraplegia type 17,
Silver spastic paraplegia syndrome,
spastic paraplegia-amyotrophy of hands and feet

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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