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Term:Milner Khallouf Gibson Syndrome
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Accession:DOID:9008423 term browser browse the term
Synonyms:primary_id: MESH:C537473;   RDO:0003318
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  disease 15599
    syndrome 5135
      Milner Khallouf Gibson Syndrome 0
Path 2
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  disease 15599
    Developmental Diseases 8726
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7507
        genetic disease 6997
          monogenic disease 4558
            autosomal genetic disease 3509
              autosomal dominant disease 2076
                complex cortical dysplasia with other brain malformations 479
                  Malformations of Cortical Development, Group I 335
                    microcephaly 207
                      Milner Khallouf Gibson Syndrome 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.