OBO ID: DOID:0060830 |
Term Name: | deafness-intellectual disability, Martin-Probst type syndrome | Search Ontology: | |
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Definition: | A syndromic X-linked intellectual disability characterized by severe bilateral deafness, intellectual disability, umbilical hernia and abnormal dermatoglyphics that has_material_basis_in variation on the X chromosome. https://www.ncbi.nlm.nih.gov/pubmed/11073537 | ||
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Ontology: | Human Disease ( DOID:0060830 ) |
OTHER deafness-intellectual disability, Martin-Probst type syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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