modern wellness · Symptom
Compulsive behaviors
🩺 HPO Source
HPO ID
HPO Label
Compulsive behaviors
HPO Definition
Behavior that consists of repetitive acts, characterized by the feeling that one "has to" perform them, while being aware that these acts are not in line with one's overall goal.
🔤 Synonyms (7)
Synonyms
Obsessive compulsive behaviorObsessive compulsive behaviourObsessive compulsive disorderObsessive-compulsive behaviorObsessive-compulsive behaviourObsessive-compulsive disorderOCD
🔗 Cross-References (4)
SNOMEDCT_US12479006
SNOMEDCT_US191736004
UMLSC0028768
UMLSC0600104
🔼 Broader Terms (1)
HP:5200241Recurrent maladaptive behavior
🏥 Conditions where Compulsive behaviors appears
35 · bridged via HPO ↔ OMIM
syndrome OMIM 615873
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder
freq: 1/10 ev: PCS
syndrome OMIM 300842
Blood Group Deletion Syndrome
ev: PCS
syndrome OMIM 613174
Chromosome 5P13 Duplication Syndrome
freq: 1/6 ev: PCS
syndrome OMIM 261600
Classical Phenylketonuria
ev: TAS
syndrome OMIM 135900
Coffin-Siris Syndrome
freq: HP:0040284 ev: IEA
syndrome OMIM 618027
Coffin-Siris Syndrome 7
freq: 1/8 ev: PCS
syndrome OMIM 266265
Congenital Disorder of Glycosylation, Type 2C
freq: 1/2 ev: PCS
syndrome OMIM 309548
Fraxe Syndrome
ev: TAS
syndrome OMIM 137580
Gilles De La Tourette Syndrome
ev: IEA
syndrome OMIM 261600
Hyperphenylalaninemia, Non-Pku Mild
ev: TAS
syndrome OMIM 617450
Intellectual Developmental Disorder With Gastrointestinal Difficulties And High Pain Threshold
freq: 1/14 ev: PCS
syndrome OMIM 610253
Kleefstra Syndrome 1
freq: 9/104 ev: PCS
syndrome OMIM 309520
Lujan Fryns Syndrome
ev: IEA
syndrome OMIM 613670
Mental Retardation With Language Impairment And With Or Without Autistic Features
freq: 3/3 ev: PCS
syndrome OMIM 135900
Mental Retardation, Autosomal Dominant 12
freq: HP:0040284 ev: IEA
syndrome OMIM 615502
Mental Retardation, Autosomal Dominant 21
freq: 1/46 ev: PCS
syndrome OMIM 615761
Mental Retardation, Autosomal Dominant 23
freq: 3/7 ev: PCS
syndrome OMIM 617061
Mental Retardation, Autosomal Dominant 44
freq: 3/12 ev: PCS
syndrome OMIM 618050
Mental Retardation, Autosomal Dominant 57
ev: IEA
syndrome OMIM 616269
Mental Retardation, Autosomal Recessive 48
freq: 2/5 ev: PCS
syndrome OMIM 300114
Mental Retardation, X-Linked 15
ev: IEA
syndrome OMIM 300114
Mental Retardation, X-Linked 49
ev: IEA
syndrome OMIM 300919
Mental Retardation, X-Linked 99
freq: 1/5 ev: PCS
syndrome OMIM 300986
Mental Retardation, X-Linked, Syndromic, Bain Type
freq: 1/6 ev: PCS
syndrome OMIM 614852
Microcephaly 9, Primary, Autosomal Recessive
freq: 1/3 ev: PCS
syndrome OMIM 615157
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
ev: TAS
syndrome OMIM 159900
Myoclonic Dystonia
freq: 1/37 ev: PCS
syndrome OMIM 615643
Neurodegeneration With Brain Iron Accumulation 6
freq: 1/2 ev: PCS
disease OMIM 164230
Obsessive-Compulsive Disorder
ev: IEA
syndrome OMIM 615722
Optic Atrophy, Intellectual Disability Syndrome
freq: 1/6 ev: PCS
syndrome OMIM 261600
Phenylketonuria, Maternal
ev: TAS
syndrome OMIM 614558
Scn8A-Related Epilepsy With Encephalopathy
freq: 1/1 ev: PCS
syndrome OMIM 617044
Short Stature, Developmental Delay, And Congenital Heart Defects
freq: 2/5 ev: PCS
disease OMIM 613229
Trichotillomania
ev: IEA
syndrome OMIM 612469
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome
freq: 1/2 ev: PCS