Deafness - intellectual deficit syndrome, Martin-Probst type (Q58756): Difference between revisions
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Revision as of 06:19, 14 August 2026
Martin-Probst syndrome is characterised by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_458131527 |
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| English | Deafness - intellectual deficit syndrome, Martin-Probst type |
Martin-Probst syndrome is characterised by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics. |
Statements
CID11:ID_458131527
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