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DOID:0060830 - deafness-intellectual disability, Martin-Probst type syndrome
Disease Ontology 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.
Synonyms: Martin-Probst syndrome, mental retardation, X-linked, syndromic, Martin-Probst type,
Xenbase Genes :
MONDO:0010353 - deafness-intellectual disability, Martin-Probst type syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee