Filippi syndrome (Q94166): Difference between revisions
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15 August 2026
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Latest revision as of 09:17, 16 August 2026
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1989471300 |
||
| English | Filippi syndrome |
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline). |
Statements
CID11:ID_1989471300
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dki-india-ID_1989471300
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Concluído
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15 August 2026
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