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

93282000: Congenital hypoplasia of parietal 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
154359015 Congenital hypoplasia of parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154360013 Congenital small parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836983018 Congenital hypoplasia of parietal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154359015 Congenital hypoplasia of parietal bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154359015 Congenital hypoplasia of parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154360013 Congenital small parietal bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154360013 Congenital small parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836983018 Congenital hypoplasia of parietal bone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836983018 Congenital hypoplasia of parietal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4709191000241110 hypoplasie de l'os pariétal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4709191000241110 hypoplasie de l'os pariétal 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 parietal bone Is a Congenital anomaly of parietal bone (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Finding site Parietal bone structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of parietal bone Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of parietal bone Finding site Parietal bone structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of parietal bone Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of parietal bone Finding site Parietal bone structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of parietal bone Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal bone Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of parietal 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