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
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