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DOID:2476 - hereditary spastic paraplegia
Disease Ontology Definition:A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.
Synonyms: French settlement disease, Strumpell-Lorrain disease, familial spastic paraplegia, hereditary spastic paraparesis,
Xenbase Genes
:
reep1,
rtn2,
ap4s1,
fars2,
entpd1,
atl1,
spast,
ap4b1,
erlin2,
bscl2,
pnpla6,
kif1a,
b4galnt1,
tfg,
reep2,
| MONDO:0019064 - hereditary spastic paraplegia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
paraplegia (is_a)