GINGF2 gene related symptoms and diseases

All the information presented here about the GINGF2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to GINGF2 gene

Symptoms // Phenotype % Cases
Overgrowth Very Common - Between 80% and 100% cases
Hypertrichosis Very Common - Between 80% and 100% cases
Gingival overgrowth Very Common - Between 80% and 100% cases
Gingival fibromatosis Very Common - Between 80% and 100% cases

Rare diseases associated to GINGF2 gene

Here you will find a list of rare diseases related to the GINGF2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


HEREDITARY GINGIVAL FIBROMATOSIS

Alternate names

HEREDITARY GINGIVAL FIBROMATOSIS Is also known as autosomal dominant gingival fibromatosis, ggf1, autosomal dominant gingival hyperplasia, gingf, hereditary gingival hyperplasia, fibromatosis, gingival, hereditary, hgf

Description

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.

Most common symptoms of HEREDITARY GINGIVAL FIBROMATOSIS

  • Overgrowth
  • Hypertrichosis
  • Gingival overgrowth
  • Gingival fibromatosis


More info about HEREDITARY GINGIVAL FIBROMATOSIS

SOURCES: OMIM ORPHANET



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