CECR - cat eye syndrome chromosome region Gene

Also Known as CES

Species: Homo sapiens

Gene Type: other
Gene ID: 1055

About CECR

Cytogenetic location: 22q11 Genomic coordinates (GRCh38): 22:15,000,001-25,500,000

Summary

Cat eye syndrome (CES) is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. A small supernumerary chromosome (smaller than chromosome 21) is present, frequently has 2 centromeres, is bisatellited, and represents an inv dup(22)(q11).[supplied by OMIM, Aug 2009]

Related Diseases

Diseases Alias
Cat Eye Syndrome
  • CES

  • Schmid-Fraccaro Syndrome

  • Chromosome 22 Partial Tetrasomy

  • Inv Dup(22)(Q11)

  • Cat-Eye Syndrome

  • Cess

  • Opitz Trigonocephaly Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma