7p2 monosomy syndrome

Preferred Label : 7p2 monosomy syndrome;

CISMeF synonym : chromosome 7, monosomy 7p2; chromosome 7, partial monosomy 7p; chromosome 7, terminal 7p deletion (del 7p21-p22);

Related MeSH term : Chromosome 7, partial deletion of short arm (7p2-);

Details

Origin ID

C537818;

UMLS CUI

C2931626;

CISMeF manual mappings
- 7p partial monosomy syndrome [SNOMED Notion]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 7 [MeSH Descriptor]
Record concept(s)
- 7p2 monosomy syndrome [MeSH concept]
- chromosome 7, monosomy 7p2 [MeSH concept]
- chromosome 7, partial monosomy 7p [MeSH concept]
- chromosome 7, terminal 7p deletion (del 7p21-p22) [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- 7p partial monosomy syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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