Disease #00011 (COMT (Schizophrenia), OMIM:116790)
Official abbreviation |
COMT |
Name |
Schizophrenia |
OMIM ID |
116790 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
AKT1 |
Associated tissues |
brain |
Disease features |
- |
Remarks |
- |
Date created |
2017-11-21 08:52:15 +08:00 (CST) |
Date last edited |
2021-02-25 09:31:04 +08:00 (CST) |
Individuals
|
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