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Disease Ontology Browser
hereditary spastic paraplegia 39 (DOID:0110790)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 39; autosomal recessive spastic paraplegia type 39; NTE-related motor neuron disorder; NTEMND; spastic paraplegia due to neuropathy target esterase mutation; spastic paraplegia due to NTE mutation; SPG39
Alt IDs: OMIM:612020, ICD10CM:G11.4, ORDO:139480
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory