Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0345427
Disease: Woolly hair, congenital
Woolly hair, congenital
0.300 GermlineCausalMutation disease ORPHANET Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan. 21426374 2011