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778069004: Autosomal dominant prognathism of mandible (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3737626014 Autosomal dominant prognathism of mandible (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737627017 Autosomal dominant prognathism of mandible en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737628010 Autosomal dominant mandibular prognathism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737625013 A rare genetic developmental defect during embryogenesis disorder with characteristics of abnormal forward projection of the mandible beyond the standard relation to the cranial base, with lower incisors often overlapping the upper incisors, that is inherited in an autosomal dominant manner. Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3737626014 Autosomal dominant prognathism of mandible (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737627017 Autosomal dominant prognathism of mandible en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737628010 Autosomal dominant mandibular prognathism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737625013 A rare genetic developmental defect during embryogenesis disorder with characteristics of abnormal forward projection of the mandible beyond the standard relation to the cranial base, with lower incisors often overlapping the upper incisors, that is inherited in an autosomal dominant manner. Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450821001000119 Prognathie, autosomal-dominante de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806871000241119 prognathisme autosomique dominant de la mandibule fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806881000241117 prognathisme mandibulaire autosomique dominant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806891000241115 prognathisme autosomique dominant du maxillaire inférieur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806871000241119 prognathisme autosomique dominant de la mandibule fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806881000241117 prognathisme mandibulaire autosomique dominant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5806891000241115 prognathisme autosomique dominant du maxillaire inférieur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3450821001000119 Prognathie, autosomal-dominante 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
Autosomal dominant prognathism of mandible (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant prognathism of mandible (disorder) Is a Congenital anomaly of mandible true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant prognathism of mandible (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant prognathism of mandible (disorder) Is a Mandibular prognathism true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant prognathism of mandible (disorder) Associated morphology Protrusion true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant prognathism of mandible (disorder) Finding site Bone structure of mandible true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant prognathism of mandible (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant prognathism of mandible (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant prognathism of mandible (disorder) Is a Congenital prognathism true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant prognathism of mandible (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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