Cure My Disease

Don't miss your cure!

 Log in / Sign up

Hereditary gingival fibromatosis

MONDO:0016070

Hereditary gingival fibromatosis (HGF) is a rare benign, slowly progressive, non-inflammatory fibrous hyperplasia of the maxillary and mandibular gingivae that generally occurs with the eruption of the permanent (or more rarely the primary) dentition or even at birth. It presents as a localized or generalized, smooth or nodular overgrowth of the gingival tissues of varying severity. It can be isolated, with autosomal dominant inheritance, or as part of a syndrome.

Also known as: autosomal dominant gingival fibromatosis, autosomal dominant gingival hyperplasia, hereditary gingival fibromatosis, hereditary gingival hyperplasia

22 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Fibromatosis, gingival, 2 (2) Fibromatosis, gingival, 1 (0) Fibromatosis, gingival, 3 (0) Fibromatosis, gingival, 4 (0) Fibromatosis, gingival, 5 (0) Fibromatosis, gingival, 6 (0)

Broader categories

Disease (680) Periodontal disorder (281) Musculoskeletal system disorder (207) Hereditary disease (176) Gingival disorder (24) Mouth disorder (20) Gingival overgrowth (19) Human disease (14) Mouth mucosa disorder (4) Skeletal system disorder (4)
Trials to join now! 6 Not yet recruiting 7 Not yet finished but already full! 5 Completed 4
Sort by