chromosome 9p deletion syndrome

Preferred Label : chromosome 9p deletion syndrome;

MeSH synonym : monosomy 9p; monosomy 9p syndrome; chromosome 9, monosomy 9p; Deletion 9p Syndrome;

Détails

Origin ID

C538024;

UMLS CUI

C0795830;

Automatic exact mappings (from CISMeF team)
- 9p partial monosomy syndrome (disorder) [Inactive SNOMED CT concept]
Currated CISMeF NLP mapping
- Alfi syndrome [ICD-11 More detail]
- Chromosome 9p deletion syndrome [OMIM Phenotype]
- Monosomy 9p [ORDO Disease]
- Monosomy 9p (disorder) [SNOMED CT concept]
- chromosome 9p deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 9 [MeSH Descriptor]
Record concept(s)
- Deletion 9p [MeSH concept]
- chromosome 9p deletion syndrome [MeSH concept]
See also inter- (CISMeF)
- Distal monosomy 9p [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alfi syndrome [ICD-11 More detail]
- Chromosome 9p deletion syndrome [OMIM Phenotype]
- Monosomy 9p [ORDO Disease]
- Monosomy 9p (disorder) [SNOMED CT concept]
- chromosome 9p deletion syndrome [DO Concept]

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