proximal upper limb amyotrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy affecting proximally located muscles of the arms. (Human Phenotype Ontology, HP_0008948)
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2 genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HNRNPDL heterogeneous nuclear ribonucleoprotein D-like
TCAP titin-cap