Deafness - intellectual deficit syndrome, Martin-Probst type (Q58756)

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Martin-Probst syndrome is characterised by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics.
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ID_458131527
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    Deafness - intellectual deficit syndrome, Martin-Probst type
    Martin-Probst syndrome is characterised by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics.

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      CID11:ID_458131527
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      dki-india-ID_458131527
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      Concluído
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      13 August 2026
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