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109620006: Hereditary gingival fibromatosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
174251019 Hereditary gingival fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
340227010 Hereditary fibrous enlargement of gingiva en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
613866010 Hereditary gingival fibromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
873261000172116 fibromatose gingivale héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1014071000172114 fibromatose gingivale autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3438701001000117 Gingivale Fibromatose, hereditäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary gingival fibromatosis Is a Digestive system hereditary disorder true Inferred relationship Some
Hereditary gingival fibromatosis Is a Autosomal hereditary disorder true Inferred relationship Some
Hereditary gingival fibromatosis Is a Gingival fibromatosis true Inferred relationship Some
Hereditary gingival fibromatosis Associated morphology Fibroepithelial hyperplasia false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Periodontal tissues structure false Inferred relationship Some
Hereditary gingival fibromatosis Associated morphology Fibromatosis false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Jaw region structure false Inferred relationship Some
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 2
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 2
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 2
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure false Inferred relationship Some 2
Hereditary gingival fibromatosis Associated morphology Hypertrophy false Inferred relationship Some 1
Hereditary gingival fibromatosis Finding site Gingival structure true Inferred relationship Some 1
Hereditary gingival fibromatosis Associated morphology Fibromatosis true Inferred relationship Some 1
Hereditary gingival fibromatosis Associated morphology Hypertrophy false Inferred relationship Some 1
Hereditary gingival fibromatosis Is a Gingival disease with an aetiology other than dental plaque, such as bacterial, viral, fungal or genetic origin, due to systemic conditions, trauma, foreign body reactions, or other causes. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
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. Is a True Hereditary gingival fibromatosis Inferred relationship Some
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a True Hereditary gingival fibromatosis Inferred relationship Some
A rare syndrome characterized by gingival fibromatosis associated with progressive sensorineural hearing loss. It has been described in two families (with at least 16 affected members spanning five generations in one of the families, and five affected members spanning three generations in the other family). It is transmitted as an autosomal dominant trait. Is a True Hereditary gingival fibromatosis Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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US English

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