Oral-facial-digital syndrome type 8 (Q63068): Difference between revisions
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Revision as of 10:33, 14 August 2026
Oral-facial-digital (OFD) syndrome, type 8 is a malformation syndrome characterised by tongue lobulation, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibiae and/or radii, short stature, hypoplasia of the epiglottis, duplication of the halluces and mild intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1948779753 |
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| English | Oral-facial-digital syndrome type 8 |
Oral-facial-digital (OFD) syndrome, type 8 is a malformation syndrome characterised by tongue lobulation, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibiae and/or radii, short stature, hypoplasia of the epiglottis, duplication of the halluces and mild intellectual deficit. |
Statements
CID11:ID_1948779753
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