chromosome 1p36 deletion syndrome

Preferred Label : chromosome 1p36 deletion syndrome;

CISMeF synonym : 1p36.33 deletion;

MeSH synonym : 1p36 deletion syndrome; monosomy 1p36 syndrome; chromosome 1, 1p36 deletion syndrome;

Related MeSH term : Deletion 1p36.33;

Details

Origin ID

C535362;

UMLS CUI

C1842870;

Automatic exact mappings (from CISMeF team)
- 1p36 deletion syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- 1p36 Deletion Syndrome [NCIt concept]
- 1p36 deletion [ICD-11 More detail]
- 1p36 deletion syndrome [ORDO Disease]
- Chromosome 1p36 deletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 1p36 deletion syndrome, distal [OMIM Phenotype]
- chromosome 1p36 deletion syndrome [DO Concept]
- chromosome 1p36 deletion syndrome [Disease (Nov.)]
DO Cross reference
- chromosome 1p36 deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 1 [MeSH Descriptor]
Record concept(s)
- 1p36.33 deletion [MeSH concept]
- chromosome 1p36 deletion syndrome [MeSH concept]
See also inter- (CISMeF)
- del(1p36) [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 1p36 Deletion Syndrome [NCIt concept]
- 1p36 deletion [ICD-11 More detail]
- 1p36 deletion syndrome [ORDO Disease]
- 1p36 deletion syndrome [MedDRA Preferred Term]
- Chromosome 1p36 deletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 1p36 deletion syndrome, distal [OMIM Phenotype]
- chromosome 1p36 deletion syndrome [DO Concept]
- chromosome 1p36 deletion syndrome [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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