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 |
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