DISEASES

Disease-gene associations mined from literature

Human genes for deafness-intellectual disability, Martin-Probst type syndrome

Deafness-intellectual disability, Martin-Probst type syndrome [DOID:0060830]

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:  deafness-intellectual disability, Martin-Probst type syndrome,  deafnessintellectual disability MartinProbst type syndrome,  deafness-intellectual disability, Martin-Probst type disease,  deafness-intellectual disability, Martin-Probst type disorder,  DOID:0060830 ...