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X-linked congenital generalized hypertrichosis

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0010614:  X-linked congenital generalized hypertrichosis
GARD:0002863: 
MESH:C538388: 
Orphanet:79495: