Disease #00078
Official abbreviation |
SGBS1 |
Name |
Simpson-Golabi-Behmel syndrome, type 1 |
OMIM ID |
312870 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
GPC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|