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770760006: 16q24.1 microdeletion syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3702490014 16q24.1 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3702491013 16q24.1 microdeletion syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3702492018 Monosomy 16q24.1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404921018 A partial autosomal monosomy characterized clinically by lethal pulmonary disease that presents as severe respiratory distress and refractory pulmonary hypertension within a few hours after birth and typically results in death from respiratory failure within the first months of life. Characteristic histological features of lung tissue include paucity of alveolar wall capillaries, alveolar wall thickening, muscular hypertrophy of the pulmonary arteries, and malposition of the small pulmonary veins. Various additional congenital malformations may be associated, mostly gastrointestinal (intestinal malrotation and atresias, anular pancreas), genitourinary (dilatation of urinary tracts, duplicated uterus) and cardiovascular anomalies (hypoplastic left heart and other congenital heart defects). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404922013 A partial autosomal monosomy characterised clinically by lethal pulmonary disease that presents as severe respiratory distress and refractory pulmonary hypertension within a few hours after birth and typically results in death from respiratory failure within the first months of life. Characteristic histological features of lung tissue include paucity of alveolar wall capillaries, alveolar wall thickening, muscular hypertrophy of the pulmonary arteries, and malposition of the small pulmonary veins. Various additional congenital malformations may be associated, mostly gastrointestinal (intestinal malrotation and atresias, anular pancreas), genitourinary (dilatation of urinary tracts, duplicated uterus) and cardiovascular anomalies (hypoplastic left heart and other congenital heart defects). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
16q24.1 microdeletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
16q24.1 microdeletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
16q24.1 microdeletion syndrome (disorder) Is a 16q partial monosomy syndrome false Inferred relationship Some
16q24.1 microdeletion syndrome (disorder) Finding site Chromosome pair 16 false Inferred relationship Some 1
16q24.1 microdeletion syndrome (disorder) Is a Interstitial lung disease true Inferred relationship Some
16q24.1 microdeletion syndrome (disorder) Finding site Chromosome pair 16 true Inferred relationship Some 2
16q24.1 microdeletion syndrome (disorder) Finding site Structure of interstitial tissue of lung true Inferred relationship Some 3
16q24.1 microdeletion syndrome (disorder) Is a Congenital connective tissue disorder true Inferred relationship Some
16q24.1 microdeletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
16q24.1 microdeletion syndrome (disorder) Associated morphology Deletion of long arm false Inferred relationship Some 2
16q24.1 microdeletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
16q24.1 microdeletion syndrome (disorder) Is a Partial deletion of long arm of chromosome 16 true Inferred relationship Some
16q24.1 microdeletion syndrome (disorder) Is a Congenital malformation true Inferred relationship Some
16q24.1 microdeletion syndrome (disorder) Finding site Long arm of chromosome true Inferred relationship Some 1
16q24.1 microdeletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
16q24.1 microdeletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 2
16q24.1 microdeletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
16q24.1 microdeletion syndrome (disorder) Is a Respiratory condition of fetus OR newborn true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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