Disease #03608 (SCZD17 (schizophrenia, type 17 (SCZD17)), OMIM:614332)
| Official abbreviation |
SCZD17 |
| Name |
schizophrenia, type 17 (SCZD17) |
| OMIM ID |
614332 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
NRXN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-07-21 14:11:39 +02:00 (CEST) |
Individuals
|