Summary Literature (0)

DOID:0110790 - hereditary spastic paraplegia 39

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13.

Synonyms: NTE-related motor neuron disorder, NTEMND, SPG39, autosomal recessive spastic paraplegia 39, autosomal recessive spastic paraplegia type 39, spastic paraplegia due to NTE mutation, spastic paraplegia due to neuropathy target esterase mutation,

Echinobase Genes :


OMIM:

MIM:612020 - spastic paraplegia 39, autosomal recessive; spg39

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

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