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17608003: CHILD-syndroom (aandoening)


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
5278070017 Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5278071018 Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5278072013 CHILD syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5278073015 CHILD (congenital hemidysplasia, ichthyosiform erythroderma, limb defects) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
341041000146117 CHILD-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
341051000146119 CHILD-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5278074014 A rare developmental defect during embryogenesis with characteristics of unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies. NSDHL (Xq28) encodes a protein responsible for cholesterol biosynthesis, mutations are typically lethal in males. X-inactivation creates a mosaic of cells lacking the enzyme in females, disrupting embryonic development and leading to a highly variable spectrum of anomalies. Transmission is X-linked dominant. 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
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Occurrence Congenital false Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 1
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Congenital anomaly of skin true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Congenital ichthyosiform erythroderma true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Disorder of lipid metabolism true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Congenital anomaly of limb true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Is a Inborn error of metabolism true Inferred relationship Some
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Interprets Keratinization true Inferred relationship Some 3
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Has interpretation Abnormal true Inferred relationship Some 3
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Finding site Skin structure true Inferred relationship Some 1
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Finding site Limb structure true Inferred relationship Some 2
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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