deafness-intellectual disability, Martin-Probst type syndrome Disease Ontology Browser

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deafness-intellectual disability, Martin-Probst type syndrome (DOID:0060830)
Alliance: disease page
Synonyms: Martin-Probst syndrome; mental retardation, X-linked, syndromic, Martin-Probst type
Alt IDs: OMIM:300519, ICD10CM:Q87.8, ORDO:85321
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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