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254026007: Craniofacial microsomia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378165017 Craniofacial microsomia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644861018 Craniofacial microsomia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
378165017 Craniofacial microsomia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378165017 Craniofacial microsomia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644861018 Craniofacial microsomia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644861018 Craniofacial microsomia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5081241000241115 microsomie craniofaciale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5081241000241115 microsomie craniofaciale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

43 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniofacial microsomia (disorder) Is a Congenital anomaly of face bones false Inferred relationship Existential restriction modifier (core metadata concept)
Craniofacial microsomia (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Finding site Cartilaginous tissue structure false Inferred relationship Existential restriction modifier (core metadata concept)
Craniofacial microsomia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Craniofacial microsomia (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniofacial microsomia (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniofacial microsomia (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniofacial microsomia (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniofacial microsomia (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniofacial microsomia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniofacial microsomia (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniofacial microsomia (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniofacial microsomia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniofacial microsomia (disorder) Is a Congenital abnormality of skull and face bones (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Craniofacial microsomia (disorder) Finding site Bone structure of head true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Antley-Bixler syndrome Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral craniofacial microsomia (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Acrorenal mandibular syndrome (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome Is a False Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hemifacial microsomia (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital micrognathism Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of zygomatic bone (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital alveolar hypoplasia of mandible Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Goldenhar syndrome (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital maxillary hypoplasia Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of nasal bone (disorder) Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of alisphenoid bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of basioccipital bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of exoccipital bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of frontal bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of interparietal bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of lacrimal bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of squamosal bone Is a True Craniofacial microsomia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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