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93284004: Congenital hypoplasia of premaxilla (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
154364016 Congenital hypoplasia of premaxilla en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154365015 Congenital small premaxilla en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836985013 Congenital hypoplasia of premaxilla (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154364016 Congenital hypoplasia of premaxilla en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154364016 Congenital hypoplasia of premaxilla en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154365015 Congenital small premaxilla en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154365015 Congenital small premaxilla en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836985013 Congenital hypoplasia of premaxilla (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836985013 Congenital hypoplasia of premaxilla (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4709211000241114 hypoplasie congénitale de l'os prémaxillaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4709211000241114 hypoplasie congénitale de l'os prémaxillaire 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 premaxilla (disorder) Is a Congenital anomaly of premaxilla true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of premaxilla (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of premaxilla (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Finding site Cartilaginous tissue structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of premaxilla (disorder) Finding site Structure of premaxillary bone true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of premaxilla (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of premaxilla (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of premaxilla (disorder) Is a Congenital anomaly of face bones false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of premaxilla (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Finding site Structure of premaxillary bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Finding site Bone structure of face false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of premaxilla (disorder) Finding site Structure of premaxillary bone false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of premaxilla (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of premaxilla (disorder) Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of premaxilla (disorder) 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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