FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

719687007: Gingival fibromatosis with facial dysmorphism syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5402205019 A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402206018 A very rare syndrome characterised by the association of gingival fibromatosis and craniofacial dysmorphism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3317490016 Gingival fibromatosis with facial dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3317491017 Gingival fibromatosis with facial dysmorphism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1006641000172116 syndrome de fibromatose gingivale-dysmorphie faciale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3410681001000112 Gingivale Fibromatose-Gesichtsdysmorphie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a Autosomal recessive hereditary disorder true Inferred relationship Some
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a Hereditary gingival fibromatosis true Inferred relationship Some
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology anomalie du développement false Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Occurrence Congenital false Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Finding site Face structure false Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology Fibromatosis false Inferred relationship Some 3
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Finding site Gingival structure false Inferred relationship Some 3
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology Fibromatosis true Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Finding site Gingival structure true Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Occurrence Congenital true Inferred relationship Some 1
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Finding site Face structure true Inferred relationship Some 1
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a Developmental hereditary disorder true Inferred relationship Some
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start