Summary Literature (0)

DOID:0110824 - hereditary spastic paraplegia 9A

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ALDH18A1 gene on chromosome 10q24.

Synonyms: AD-SPG9A, Cataracts motor neuropathy-short stature-skeletal anomalies syndrome, SPG9A, autosomal dominant complex spastic paraplegia type 9A, autosomal dominant spastic paraplegia 9A, cataracts with motor neuronopathy, short stature and skeletal abnormalities, spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux, spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee