congenital hemidysplasia with ichthyosiform erythroderma and limb defects

Preferred Label : congenital hemidysplasia with ichthyosiform erythroderma and limb defects;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0562815;

UMLS CUI

C0265267;

Automatic exact mappings (from CISMeF team)
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects [MedDRA LLT]
Currated CISMeF NLP mapping
- CHILD syndrome [Disease (Nov.)]
- CHILD syndrome [ORDO Disease]
- Child syndrome (disorder) [SNOMED CT concept]
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects [OMIM Phenotype]
- Congenital hemidysplasia with ichthyosiform erythroderma and limbs defects [ICD-11 More detail]
- child syndrome [SNOMED Notion]
Related record
- congenital hemidysplasia with ichthyosiform erythroderma and limb defects [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CHILD syndrome [ORDO Disease]
- CHILD syndrome [Disease (Nov.)]
- CHILD syndrome [MedDRA Preferred Term]
- CHILD syndrome [DO Concept]
- Child syndrome (disorder) [SNOMED CT concept]
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects [OMIM Phenotype]
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects [MedDRA LLT]
- Congenital hemidysplasia with ichthyosiform erythroderma and limbs defects [ICD-11 More detail]
- child syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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