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93281007: Congenital hypoplasia of palatine 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
154357018 Congenital hypoplasia of palatine bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154358011 Congenital small palatine bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836982011 Congenital hypoplasia of palatine bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154357018 Congenital hypoplasia of palatine bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154357018 Congenital hypoplasia of palatine bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154358011 Congenital small palatine bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154358011 Congenital small palatine bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836982011 Congenital hypoplasia of palatine bone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836982011 Congenital hypoplasia of palatine bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5900501000241116 hypoplasie congénitale de l'os palatin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5900501000241116 hypoplasie congénitale de l'os palatin 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 palatine bone Is a Congenital anomaly of palatine bone true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Finding site Cartilaginous tissue structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Finding site Palatine bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Finding site Palatine bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Is a Congenital malformation of upper alimentary tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of palatine bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of palatine bone Finding site Palatine bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of palatine bone Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of palatine bone Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine bone Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of palatine 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

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