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DOID:0060896 - autosomal recessive early-onset Parksinson disease 23
Disease Ontology Definition:An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
Synonyms:
Xenbase Genes : vps13c
MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
early-onset Parkinson's disease (is_a)