7p2 monosomy syndrome - CISMeF

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CISMeF

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7p2 monosomy syndromeMeSH concept

Preferred Label : 7p2 monosomy syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0535855;

UMLS CUI

C2931626;

Related MeSH concept(s)
- chromosome 7, monosomy 7p2 [MeSH concept]
- chromosome 7, partial monosomy 7p [MeSH concept]
- chromosome 7, terminal 7p deletion (del 7p21-p22) [MeSH concept]
Related record
- 7p2 monosomy syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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05/05/2025

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