Greig cephalopolysyndactyly syndrome (Q84223): Difference between revisions
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Revision as of 09:34, 15 August 2026
Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_606500237 |
||
| English | Greig cephalopolysyndactyly syndrome |
Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands. |
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CID11:ID_606500237
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dki-india-ID_606500237
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Concluído
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