skeletal muscle hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or decreased size of the skeletal muscle, usually due an decreased number of cells (Mammalian Phenotype Ontology, MP_0009460)
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2 gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
NF1 neurofibromin 1