FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

93293003: Congenital hypoplasia of squamosal bone (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
154384017 Congenital hypoplasia of squamosal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154385016 Congenital small squamosal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836996017 Congenital hypoplasia of squamosal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154384017 Congenital hypoplasia of squamosal bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154384017 Congenital hypoplasia of squamosal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154385016 Congenital small squamosal bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154385016 Congenital small squamosal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836996017 Congenital hypoplasia of squamosal bone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836996017 Congenital hypoplasia of squamosal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4709331000241112 hypoplasie congénitale de l'écaille du temporal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4709331000241112 hypoplasie congénitale de l'écaille du temporal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of squamosal bone Is a Congenital anomaly of squamosal bone (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of squamosal bone Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of squamosal bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of squamosal bone Finding site Structure of squamous part of temporal bone true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of squamosal bone Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of squamosal bone Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of squamosal bone Finding site Structure of squamous part of temporal bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of squamosal bone Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of squamosal bone Finding site Structure of squamous part of temporal bone false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of squamosal bone Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of squamosal bone Is a Craniofacial microsomia (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

Back to Start