midclavicular aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental defect resulting in congenital absence of the middle portion of the clavicle. (Human Phenotype Ontology, HP_0006638)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006638
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Genes

1 genes associated with the midclavicular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PORCN porcupine homolog (Drosophila)