anemic pallor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of pallor that is secondary to the presence of anemia. (Human Phenotype Ontology, HP_0001017)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001017
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Genes

4 genes associated with the anemic pallor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FANCA Fanconi anemia, complementation group A
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E