Name | Simpson-Golabi-Behmel Syndrome, Type 2 |
---|---|
Synonym | SGBS2 |
Categories | Congenital abnormality | Genetic disease (inborn) |
MeSH® ID | C564567 |
OMIM® ID | 300209 |
1. |
Diseases
←
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
2. |
Diseases
←
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |