prognathism Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormal prominence of the chin related to increased length of the mandible. (Human Phenotype Ontology, HP_0000303)
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Genes

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

Symbol Name
EPB41 erythrocyte membrane protein band 4.1
GHR growth hormone receptor
MATN1 matrilin 1, cartilage matrix protein