X inactivation, familial skewed, 1 - CISMeF

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CISMeF

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X inactivation, familial skewed, 1MeSH Supplementary Concept

Preferred Label : X inactivation, familial skewed, 1;

Details

Origin ID

C564716;

UMLS CUI

C1848138;

Currated CISMeF NLP mapping
- X inactivation, familial skewed, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- x chromosome inactivation [MeSH Descriptor]
Record concept(s)
- X inactivation, familial skewed, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- X inactivation, familial skewed, 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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18/05/2024

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