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Disease Chromosome 19q13.11 Deletion Syndrome

Name Chromosome 19q13.11 Deletion Syndrome
Categories Congenital abnormality | Genetic disease (inborn) | Pathology (process)
MeSH® ID C567810
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated exposure references Abnormalities, Multiple Has associated chemicals Has associated genes Chromosome 19q13.11 Deletion Syndrome
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated exposure references Chromosome Disorders Has associated chemicals Has associated genes Chromosome 19q13.11 Deletion Syndrome
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Chromosome Disorders Has associated chemicals Has associated genes Chromosome 19q13.11 Deletion Syndrome
4. DiseasesPathological Conditions, Signs and Symptoms Has associated chemicals Has associated genes Has associated exposure references Pathologic Processes Has associated chemicals Has associated genes Has associated exposure references Chromosome Aberrations Has associated chemicals Has associated genes Has associated exposure references Aneuploidy Has associated chemicals Has associated genes Has associated exposure references Monosomy Has associated chemicals Has associated genes Chromosome Deletion Has associated chemicals Has associated genes Chromosome 19q13.11 Deletion Syndrome

Top ↑ Descendants

None.