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Disease Simpson-Golabi-Behmel Syndrome, Type 2

Name Simpson-Golabi-Behmel Syndrome, Type 2
Synonym SGBS2
Categories Congenital abnormality | Genetic disease (inborn)
MeSH® ID C564567
OMIM® ID 300209

Top ↑ Ancestors

1. Diseases ← Congenital, 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 ← Simpson-Golabi-Behmel Syndrome, Type 2 Has associated chemicals Has associated genes
2. Diseases ← Congenital, 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 ← Genetic Diseases, X-Linked Has associated chemicals Has associated genes ← Simpson-Golabi-Behmel Syndrome, Type 2 Has associated chemicals Has associated genes

Top ↑ Descendants

None.