Disease #00292 (OCD (obsessive compulsive disorder (OCD)), OMIM:164230)
Official abbreviation |
OCD |
Name |
obsessive compulsive disorder (OCD) |
OMIM ID |
164230 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
1 |
Associated with 3 genes |
BDNF, HTR2A, SLC6A4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-12-20 11:10:30 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|