Spinal Muscular Atrophies of Childhood Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A spinal muscular atrophy that is associated with the survival of motor neuron protein. (Human Disease Ontology, DOID_0060160)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014897
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Genes

2 genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SMN2 survival of motor neuron 2, centromeric 2.88009
SMN1 survival of motor neuron 1, telomeric 2.88009