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255399007: Congenital (qualifier value)

Status: current, Not 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
380598010 Congenital en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
380599019 Congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life false Inferred relationship Some
Congenital Is a Fetal and/or neonatal period true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation Occurrence True Congenital Inferred relationship Some 4
Mayer Rokitansky Küster Hauser syndrome (disorder) Occurrence True Congenital Inferred relationship Some 1
Mayer Rokitansky Küster Hauser syndrome (disorder) Occurrence True Congenital Inferred relationship Some 2
Mayer Rokitansky Küster Hauser syndrome (disorder) Occurrence True Congenital Inferred relationship Some 3
Oculogastrointestinal neurodevelopmental syndrome Occurrence True Congenital Inferred relationship Some 1
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder) Occurrence True Congenital Inferred relationship Some 1
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder) Occurrence True Congenital Inferred relationship Some 2
Renal tubulopathy with encephalopathy and liver failure syndrome (disorder) Occurrence True Congenital Inferred relationship Some 1
2p21 microdeletion syndrome without cystinuria (disorder) Occurrence True Congenital Inferred relationship Some 3
2p21 microdeletion syndrome without cystinuria (disorder) Occurrence True Congenital Inferred relationship Some 4
Hydroxymethylglutaric aciduria (disorder) Occurrence True Congenital Inferred relationship Some 1
Aromatic L-amino acid decarboxylase deficiency disorder (disorder) Occurrence True Congenital Inferred relationship Some 3

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This concept is not in any reference sets

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