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Summary Literature (0)
DOID:0060160 - childhood spinal muscular atrophy

Disease Ontology Definition:A spinal muscular atrophy that is associated with the survival of motor neuron protein in childhood and that has_material_basis_in variation in the SMN gene.

Synonyms: spinal muscular atrophies of childhood, survival motor neuron spinal muscular atrophy

Xenbase Genes : smn1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009669 - spinal muscular atrophy, type 1


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): spinal muscular atrophy (is_a)