has characteristic has characteristic X-linked congenital generalized hypertrichosis https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/2863/x-linked-congenital-generalized-hypertrichosis https://www.malacards.org/card/hypertrichosis_congenital_generalized_2 https://www.malacards.org/card/x_linked_congenital_generalized_hypertrichosis congenital generalized hypertrichosis, Macias-Flores type hypertrichosis congenital generalized X-linked 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. hypertrichosis congenital generalised X-linked OMIM:307150 GARD:0002863 Macias Flores-Garcia Cruz-Rivera syndrome MONDO:0010614 Cgh UMLS:C5887323 chromosome Xq27.1 interchromosomal insertion syndrome hCG Orphanet:79495 MEDGEN:1856186 hypertrichosis, congenital generalized HTC2 Macias-Flores Garcia-Cruz Rivera syndrome hypertrichosis, congenital generalised chromosome Xq27.1 Interchromosomal insertion syndrome congenital generalised hypertrichosis, Macias-Flores type hypertrichosis, congenital generalized, X-linked dominant MESH:C538388 hypertrichosis lanuginosa congenita congenital