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778069004: autosomaal dominante mandibulaire prognathie (aandoening)


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
6210261000146116 autosomaal dominante prognathie van onderkaak nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6210281000146112 autosomaal dominante prognathie van mandibula nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6996151000146110 autosomaal dominante mandibulaire prognathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7016111000146116 autosomaal dominante mandibulaire prognathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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


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 Some
Autosomal dominant prognathism of mandible (disorder) Is a Congenital anomaly of mandible true Inferred relationship Some
Autosomal dominant prognathism of mandible (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant prognathism of mandible (disorder) Is a Mandibular prognathism true Inferred relationship Some
Autosomal dominant prognathism of mandible (disorder) Associated morphology Protrusion true Inferred relationship Some 1
Autosomal dominant prognathism of mandible (disorder) Finding site Bone structure of mandible true Inferred relationship Some 1
Autosomal dominant prognathism of mandible (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant prognathism of mandible (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Autosomal dominant prognathism of mandible (disorder) Is a Congenital prognathism true Inferred relationship Some
Autosomal dominant prognathism of mandible (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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