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DOID:0111210 - distal hereditary motor neuronopathy type 2D
Disease Ontology Definition:A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in FBXO38 on 5q32.
Synonyms: HMN IID, HMN2D, distal hereditary motor neuropathy type IID, distal spinal muscular atrophy with calf predominance,
Echinobase Genes :
MIM:615575 - neuronopathy, distal hereditary motor, type iid; hmn2d |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee