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DOID:0110825 - hereditary spastic paraplegia 9B
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
Synonyms: SPG9B, autosomal recessive complex spastic paraplegia type 9B, autosomal recessive spastic paraplegia 9B,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee