obsolete_X-linked congenital generalized hypertrichosis true MESH:C538388 orphanet X-linked congenital generalized hypertrichosis is an extremely rare type of hypertrichosis lanuginosa congenita, a congenital skin disease, which is characterized by hair overgrowth on the entire body in males, and mild and asymmetric hair overgrowth in females. It is associated with a mild facial dysmorphism (anterverted nostrils, moderate prognathism), and, in a kindred, it was also associated with dental anomalies and deafness. ICD10:Q84.2 Macias Flores-Garcia Cruz-Rivera syndrome http://purl.obolibrary.org/obo/MONDO_0010614 UMLS:C2931836 OMIM:307150 3.41.0 Replaced with Mondo term. Congenital generalized hypertrichosis, Macias-Flores type