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93285003: Congenital hypoplasia of presphenoid 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
154366019 Congenital hypoplasia of presphenoid bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154367011 Congenital small presphenoid bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836986014 Congenital hypoplasia of presphenoid bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154366019 Congenital hypoplasia of presphenoid bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154366019 Congenital hypoplasia of presphenoid bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154367011 Congenital small presphenoid bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154367011 Congenital small presphenoid bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836986014 Congenital hypoplasia of presphenoid bone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836986014 Congenital hypoplasia of presphenoid bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4709231000241117 hypoplasie congénitale de l'os présphénoïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4709231000241117 hypoplasie congénitale de l'os présphénoïde 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 presphenoid bone Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Is a Congenital abnormality of skull and face bones (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of presphenoid bone Finding site Structure of presphenoidal bone true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Is a Congenital anomaly of presphenoid bone false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of presphenoid bone Is a Congenital abnormality of skull and face bones (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Is a anomalies fœtales congénitales false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Is a Congenital anomaly of presphenoid bone true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of presphenoid bone Finding site Structure of presphenoidal bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of presphenoid bone Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of presphenoid bone Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital hypoplasia of presphenoid bone Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital hypoplasia of presphenoid bone Finding site Structure of presphenoidal bone false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital hypoplasia of presphenoid bone Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of presphenoid bone Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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