male pseudohermaphroditism due to defective LH molecule - CISMeF

" /> male pseudohermaphroditism due to defective LH molecule - CISMeF

CISMeF

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Male pseudohermaphroditism due to defective LH moleculeMeSH Supplementary Concept

Preferred Label : male pseudohermaphroditism due to defective LH molecule;

Details

Origin ID

C535692;

UMLS CUI

C1835303;

MeSH term(s) associated for indexing
- Disorder of Sex Development, 46,XY [MeSH Descriptor]
- luteinizing hormone [MeSH Descriptor]
Record concept(s)
- male pseudohermaphroditism due to defective LH molecule [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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20/05/2025

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