sclerosis of finger phalanx Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An elevation in bone density in one or more phalanges of the fingers. Sclerosis is normally detected on a radiograph as an area of increased opacity. (Human Phenotype Ontology, HP_0100899)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100899
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Genes

4 genes associated with the sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
GJA1 gap junction protein, alpha 1, 43kDa
TRPS1 trichorhinophalangeal syndrome I