Hereditary gingival fibromatosis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Autosomal dominant gingival hyperplasia Autosomal dominant gingival fibromatosis Hereditary gingival hyperplasia |
| Number of Symptoms | 3 |
| OrphanetNr: | 2024 |
| OMIM Id: |
135300
605544 609955 611010 |
| ICD-10: |
K06.1 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic malformation syndrome with odontal and/or periodontal component
-Rare genetic disease Rare odontal or periodontal disorder -Rare genetic disease -Rare odontologic disease |
Symptom Information:
|
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(HPO:0000169) | Gingival fibromatosis | 14 / 7739 | ||||
|
|
(HPO:0000168) | Abnormality of the gingiva | Very frequent [Orphanet] | 51 / 7739 | |||
|
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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