Meacham syndrome (Q94190): Difference between revisions
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15 August 2026
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Latest revision as of 09:19, 16 August 2026
Meacham syndrome is a multiple malformation syndrome characterised by congenital diaphragmatic abnormalities, genital defects (true double vagina or septate vagina, absent uterus, abnormal male gonads in the presence of normal external female genitalia or male pseudohermaphroditism with abnormal internal female genitalia) and complex cyanotic congenital heart defects.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1307620543 |
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| English | Meacham syndrome |
Meacham syndrome is a multiple malformation syndrome characterised by congenital diaphragmatic abnormalities, genital defects (true double vagina or septate vagina, absent uterus, abnormal male gonads in the presence of normal external female genitalia or male pseudohermaphroditism with abnormal internal female genitalia) and complex cyanotic congenital heart defects. |
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CID11:ID_1307620543
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dki-india-ID_1307620543
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Concluído
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15 August 2026
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