Disease #00003 (MSX1 (Msh homeobox 1 gene), OMIM:142983)
Official abbreviation |
MSX1 |
Name |
Msh homeobox 1 gene |
OMIM ID |
142983 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 0 genes |
- |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2017-11-19 09:27:14 +08:00 (CST) |
Date last edited |
N/A |
Individuals
|
|