Deletion of short arm of chromosome 4

Preferred Label : Deletion of short arm of chromosome 4;

Inclusion CIM-10 : Wolff-Hirschorn syndrome;

Diag associé à un acte (%) : 100.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q933;

UMLS CUI

C1956097;

Automatic exact mappings (from CISMeF team)
- Chromosome 4 short arm deletion [MeSH concept]
- Deletions of the short arm of chromosome 4 [ICD-11 Sub-sub category]
- chromosome 4 short arm deletion [MeSH Supplementary Concept]
- wolf-hirschhorn syndrome [MeSH Descriptor]
DO Cross reference
- Wolf-Hirschhorn syndrome [DO Concept]
Orphanet concepts
- Autosomal monosomy [ORDO Disease]
- Partial autosomal monosomy [ORDO Disease]
- Partial deletion of the short arm of chromosome 4 [ORDO Disease]
- Wolf-Hirschhorn syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 4p partial monosomy syndrome [SNOMED Notion]
- 4p partial monosomy syndrome (disorder) [SNOMED CT concept]
- Wolf Hirchhorn Syndrome [Disease (Nov.)]
- Wolf Hirschhorn syndrome (disorder) [SNOMED CT concept]
- Wolf-Hirschhorn Syndrome [NCIt concept]
- Wolf-Hirschhorn syndrome [MedDRA Preferred Term]
- Wolf-Hirschhorn syndrome [MeSH concept]
- Wolf-Hirschhorn syndrome [ORDO Disease]
- Wolf-Hirschhorn syndrome [PASCAL descriptor]
- Wolf-Hirschhorn syndrome [DO Concept]
- Wolf-Hirschhorn syndrome [ICD-11 More detail]
- Wolf-hirschhorn syndrome [OMIM Phenotype]
- wolf-hirschhorn syndrome [MeSH Descriptor]
Validated automatic mappings to BTNT
- 4p partial monosomy syndrome (disorder) [SNOMED CT concept]
- Wolf Hirchhorn Syndrome [Disease (Nov.)]
- Wolf-Hirschhorn syndrome [DO Concept]

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