Werdnig-Hoffmann disease Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13137)
External Link http://www.omim.org/entry/253300
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Genes

2 genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
IGHMBP2 immunoglobulin mu binding protein 2
SMN1 survival of motor neuron 1, telomeric