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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
Transitional atrioventricular septal defect (disorder) Occurrence True Congenital Inferred relationship Some 3
Dicentric chromosome (disorder) Occurrence True Congenital Inferred relationship Some 1
Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate (disorder) Occurrence True Congenital Inferred relationship Some 2
EN1-related dorsoventral syndrome Occurrence True Congenital Inferred relationship Some 1
EN1-related dorsoventral syndrome Occurrence True Congenital Inferred relationship Some 2
EN1-related dorsoventral syndrome Occurrence True Congenital Inferred relationship Some 3
EN1-related dorsoventral syndrome Occurrence True Congenital Inferred relationship Some 4
Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome Occurrence True Congenital Inferred relationship Some 2
CPE-related Prader-Willi-like syndrome Occurrence True Congenital Inferred relationship Some 1
CPE-related Prader-Willi-like syndrome Occurrence True Congenital Inferred relationship Some 2
CPE-related Prader-Willi-like syndrome Occurrence True Congenital Inferred relationship Some 3
Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome (disorder) Occurrence True Congenital Inferred relationship Some 1
Non-terminal myelocystocele (disorder) Occurrence True Congenital Inferred relationship Some 1
Non-terminal myelocystocele (disorder) Occurrence True Congenital Inferred relationship Some 2
Non-terminal myelocystocele (disorder) Occurrence True Congenital Inferred relationship Some 3
Non-terminal myelocystocele (disorder) Occurrence True Congenital Inferred relationship Some 4
Congenital dysplasia of bilateral ankle joints (disorder) Occurrence True Congenital Inferred relationship Some 1
Congenital dysplasia of bilateral ankle joints (disorder) Occurrence True Congenital Inferred relationship Some 2
Transitional atrioventricular septal defect (disorder) Occurrence True Congenital Inferred relationship Some 4
Congenital deformity of musculoskeletal system (disorder) Occurrence True Congenital Inferred relationship Some 1

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This concept is not in any reference sets

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