patchy hypopigmentation of hair Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Reduced pigmentation of hair in patches. (Human Phenotype Ontology, HP_0011365)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011365
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Genes

11 genes associated with the patchy hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
EDN3	endothelin 3
EDNRB	endothelin receptor type B
KIT	v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MITF	microphthalmia-associated transcription factor
PAX3	paired box 3
PEPD	peptidase D
SNAI2	snail family zinc finger 2
SOX10	SRY (sex determining region Y)-box 10
TFAP2A	transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TMCO1	transmembrane and coiled-coil domains 1
WRN	Werner syndrome, RecQ helicase-like