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1304276001: Chromodomain helicase DNA binding protein 8 overgrowth syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5309963015 CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5309964014 Chromodomain helicase DNA binding protein 8 overgrowth syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5309966011 CHD8 overgrowth syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5309967019 Chromodomain helicase DNA binding protein 8 overgrowth syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5309965010 A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of mild to moderate intellectual disability, autism spectrum phenotype, macrocephaly, tall stature, gastrointestinal problems (including recurrent constipation), distinctive facial features (including wide-set eyes with down-slanted palpebral fissure, broad nose with full nasal tip, pointed chin and broad forehead with prominent supraorbital ridge) and sleep problems. Other clinical manifestations include anxiety problems, attention problems, impaired social interactions, and seizures. 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
CHD8 overgrowth syndrome Is a Multiple malformation syndrome with early overgrowth true Inferred relationship Some
CHD8 overgrowth syndrome Is a Neurodevelopmental disorder true Inferred relationship Some
CHD8 overgrowth syndrome Is a Genetic disease true Inferred relationship Some
CHD8 overgrowth syndrome Occurrence Congenital true Inferred relationship Some 1
CHD8 overgrowth syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
CHD8 overgrowth syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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