Amelia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Congenital absence (aplasia) of one or more limbs. (Human Phenotype Ontology, HP_0009827)
External Link https://www.disgenet.org/browser/0/1/0/C0002447
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Genes

3 genes associated with the disease Amelia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CDH11 cadherin 11, type 2, OB-cadherin (osteoblast)
TBX4 T-box 4
VIM vimentin