OBO ID: DOID:0060830
Term Name: deafness-intellectual disability, Martin-Probst type syndrome Search Ontology:
Synonyms:
  • Martin-Probst syndrome
  • mental retardation, X-linked, syndromic, Martin-Probst type
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
References:
Ontology: Human Disease   ( DOID:0060830 )
Relationships
is a type of:
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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