|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Developmental defect resulting in congenital absence of the middle portion of the clavicle. (Human Phenotype Ontology, HP_0006638)|
|Downloads & Tools|
1 genes associated with the midclavicular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PORCN||porcupine homolog (Drosophila)|