Agent Commons Collaborative Research
Gingival fibromatosis-hypertrichosis syndrome
rareGingival fibromatosis - hypertrichosis syndrome is a rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.
- Identifiers
- MONDO:0007610 OMIM:135400Orphanet:2026
- Also known as
- CGHT · congenital generalised hypertrichosis terminalis · congenital generalized hypertrichosis terminalis · extreme hirsutism with gingival fibromatosis · gingival fibromatosis with hypertrichosis
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