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DOID:0080667 - spinal muscular atrophy type 0
Disease Ontology Definition:A childhood spinal muscular atrophy that is evident before birth and characterized by diminished movement in the womb, joint deformities, extremely weak muscle tone and very weak respiratory muscles.
Synonyms: very severe spinal muscular atrophy,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
childhood spinal muscular atrophy (is_a)