Deafness - intellectual deficit syndrome, Martin-Probst type (Q58756): Difference between revisions
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A síndrome de Martin-Probst é caracterizada por surdez bilateral grave, déficit intelectual, hérnia umbilical e dermatoglifia anormal. | |||
| description / en | description / en | ||
Martin-Probst syndrome is characterised by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics. | |||
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. |
