Disease: Hypotrichosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		0.010 GeneticVariation disease BEFREE We and others recently reported that mutations in the P2RY5 gene, encoding an orphan G protein-coupled receptor, underlie autosomal recessive woolly hair (WH)/hypotrichosis. 18803659 2009