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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009669 - spinal muscular atrophy, type 1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
spinal muscular atrophy (is_a)