Oculomelic amyoplasia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Distal arthrogryposis type 5 is an inherited developmental defect syndrome characterized by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and ocular anomalies (ptosis, external ophtalmoplegia and/or strabismus). Intelligence is normal. (Orphanet Rare Disease Ontology, Orphanet_1154)
External Link http://www.omim.org/entry/108145
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Genes

1 genes associated with the Oculomelic amyoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PIEZO2 piezo-type mechanosensitive ion channel component 2