Obsessive-compulsive trait

Symptom Information:

Symptom ID: HPO:0008770
Synonyms:
Obsessive-compulsive traits [HPO:0008770]
Obsessive compulsive disorder [Orphanet:43580]
Compulsive disorder (finding) [Orphanet:43580]
Obsessive-compulsive disorder (disorder) [Orphanet:43580]
Obsessive-Compulsive Disorder [Orphanet:43580]
Compulsive disorder [Orphanet:43580]
Obsessive-compulsive trait [OMIM:Obsessive-compulsive trait]
Obsessive-compulsive traits [OMIM:Obsessive-compulsive traits]
Obsessive-compulsive disorder [Orphanet:43580]
Obsessive-compulsive disorder [MedDRA:10029898]
Compulsive conduct disorder [MedDRA:10029898]
Compulsive neurosis [MedDRA:10029898]
Compulsive reaction [MedDRA:10029898]
Obsessional neurosis [MedDRA:10029898]
Obsessional state [MedDRA:10029898]
Obsessive reaction [MedDRA:10029898]
Obsessive-compulsive disorders [MedDRA:10029898]
Obsessive-compulsive neurosis [MedDRA:10029898]
Obsessive-compulsive reaction [MedDRA:10029898]
OCD [MedDRA:10029898]
Reaction obsessive-compulsive [MedDRA:10029898]
Obsessional neurosis aggravated [MedDRA:10029898]
Quality:
Cross references:
HPO:0000722 "Obsessive-compulsive disorder" [Orphanet:43580]
Orphanet:43580 "Obsessive-compulsive disorder" [Orphanet:43580]
OMIM: "Obsessive-compulsive trait" [OMIM:Obsessive-compulsive trait]
OMIM: "Obsessive-compulsive traits" [OMIM:Obsessive-compulsive traits]
UMLS:C0028768 "Obsessive-Compulsive Disorder" [Orphanet:43580]
UMLS:C1291713 "Compulsive disorder" [Orphanet:43580]
Is a (Direct Parents):
HPO         Obsessive-compulsive behavior
MedDRA Obsessive-compulsive disorders and symptoms
Orphanet Behavioral abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Behavioral abnormality(HPO:0000708)
                   Obsessive-compulsive behavior(HPO:0000722)
                      Obsessive-compulsive trait(HPO:0008770)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Maternal hyperphenylalaninemia (Orphanet:2209)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Steinert myotonic dystrophy (Orphanet:273)
Williams syndrome (Orphanet:904)