congenital, generalized hypertrichosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A confluent, generalized overgrowth of silvery blonde to gray lanugo hair at birth. (Human Phenotype Ontology, HP_0004540)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004540
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Genes

10 genes associated with the congenital, generalized hypertrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
APCDD1 adenomatosis polyposis coli down-regulated 1
DSG4 desmoglein 4
INSR insulin receptor
LIPH lipase, member H
LMNA lamin A/C
LPAR6 lysophosphatidic acid receptor 6
RPL21 ribosomal protein L21
SNRPE small nuclear ribonucleoprotein polypeptide E
ZMPSTE24 zinc metallopeptidase STE24
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