Obsessive-compulsive behavior

Symptom Information:

Symptom ID: HPO:0000722
Synonyms:
Obsessive compulsive disorder [HPO:0000722]
Obsessive-compulsive behavior [HPO:0000722]
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 disorder [OMIM:Obsessive compulsive disorder]
Obsessive-compulsive behavior [OMIM:Obsessive-compulsive behavior]
Obsessive-compulsive disorder [OMIM:Obsessive-compulsive disorder]
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]
Obsessive compulsive behavior (1 patient) [OMIM:Obsessive compulsive behavior (1 patient)]
Quality:
Cross references:
HPO:0008770 "Obsessive-compulsive trait" [Orphanet:43580]
Orphanet:43580 "Obsessive-compulsive disorder" [Orphanet:43580]
OMIM: "Obsessive compulsive disorder" [OMIM:Obsessive compulsive disorder]
OMIM: "Obsessive-compulsive behavior" [OMIM:Obsessive-compulsive behavior]
OMIM: "Obsessive-compulsive disorder" [OMIM:Obsessive-compulsive disorder]
OMIM: "Obsessive compulsive behavior (1 patient)" [OMIM:Obsessive compulsive behavior (1 patient)]
UMLS:C0028768 "Obsessive-Compulsive Disorder" [Orphanet:43580]
UMLS:C1291713 "Compulsive disorder" [Orphanet:43580]
Is a (Direct Parents):
HPO         Behavioral abnormality
HPO         Collectionism
Orphanet Behavioral abnormality
MedDRA Obsessive-compulsive disorders and symptoms
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)
MedDRA:
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

17q21.31 microduplication syndrome (Orphanet:217340)
22q11.2 microduplication syndrome (Orphanet:1727)
2q37 microdeletion syndrome (Orphanet:1001)
5p13 microduplication syndrome (Orphanet:329802)
Alström syndrome (Orphanet:64)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 15q11.2 DELETION SYNDROME (OMIM:615656)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cornelia de Lange syndrome (Orphanet:199)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
FRAXE intellectual deficit (Orphanet:100973)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
GILLES DE LA TOURETTE SYNDROME (OMIM:137580)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
Kleefstra syndrome (Orphanet:261494)
LUJAN-FRYNS SYNDROME (OMIM:309520)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 (OMIM:615761)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Maternal hyperphenylalaninemia (Orphanet:2209)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Myoclonus-dystonia syndrome (Orphanet:36899)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 (OMIM:615643)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
OBSESSIVE-COMPULSIVE DISORDER (OMIM:164230)
Oculocerebrorenal syndrome (Orphanet:534)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Phenylketonuria (Orphanet:716)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Steinert myotonic dystrophy (Orphanet:273)
TRICHOTILLOMANIA (OMIM:613229)
Transketolase deficiency (ORPHA:488618)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)