Fuqua-Berkovitz syndrome (Q100822): Difference between revisions
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15 August 2026
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Latest revision as of 17:35, 16 August 2026
Fuqua-Berkovitz syndrome is characterised by the association of ambiguous genitalia with well-developed Mullerian structures and testes with a normal appearance.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_243268498 |
||
| English | Fuqua-Berkovitz syndrome |
Fuqua-Berkovitz syndrome is characterised by the association of ambiguous genitalia with well-developed Mullerian structures and testes with a normal appearance. |
Statements
CID11:ID_243268498
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dki-india-ID_243268498
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Concluído
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15 August 2026
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