modern wellness · Symptom

Atypical behavior

🩺 HPO Source

HPO ID

HPO Label

Atypical behavior

HPO Definition

Atypical behavior is an abnormality in a person's actions that can be controlled or modulated by the will of the individual. While abnormal behaviors can be difficult to control, they are distinct from other abnormal actions that cannot be affected by the individual's will.

HPO Curator Comment

Atypical behaviors should include or directly affect observable actions. While behavioral disorders often encompass abnormal thoughts, feelings, perceptions, or other cognitions, these alone would not be considered atypical behavioral features.

🔤 Synonyms (16)

Synonyms

Behavioral abnormalityBehavioral changesBehavioral disordersBehavioral disturbancesBehavioral problemsBehavioral symptomsBehavioral/psychiatric abnormalitiesBehavioural abnormalityBehavioural changesBehavioural disordersBehavioural disturbancesBehavioural problemsBehavioural symptomsBehavioural/Psychiatric abnormalityPsychiatric disordersPsychiatric disturbances

🔗 Cross-References (4)

SNOMEDCT_US25786006

SNOMEDCT_US277843001

UMLSC0004941

UMLSC0233514

🔼 Broader Terms (1)

HP:0011446Abnormality of mental function

🏥 Conditions where Atypical behavior appears

40 · bridged via HPO ↔ OMIM

syndrome OMIM 606232

22Q13.3 Deletion Syndrome

freq: 21/23 ev: PCS

syndrome OMIM 300100

Adrenoleukodystrophy

syndrome OMIM 300100

Adrenomyeloneuropathy

syndrome OMIM 617822

Alkuraya-Kucinskas Syndrome

syndrome OMIM 600348

Band Heterotopia

syndrome OMIM 125310

Cadasil Syndrome

syndrome OMIM 125310

Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1

syndrome OMIM 616708

Chromosome 10P12-P11 Deletion Syndrome

freq: 5/6 ev: PCS

disease OMIM 612001

Chromosome 15Q13.3 Microdeletion Syndrome

freq: 10/19 ev: PCS

phenotype OMIM 136570

Chromosome 16P12.1 Deletion Syndrome, 520-Kb

freq: 9/16 ev: PCS

phenotype OMIM 612474

Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb

freq: 1/21 ev: PCS

syndrome OMIM 611867

Chromosome 22Q11.2 Deletion Syndrome, Distal

freq: 2/6 ev: PCS

syndrome OMIM 300882

Cornelia De Lange Syndrome 5

syndrome OMIM 236200

Cystathionine Beta-Synthase Deficiency Disease

syndrome OMIM 616708

Desanto-Shinawi Syndrome

freq: 5/6 ev: PCS

syndrome OMIM 615005

Epilepsy, Nocturnal Frontal Lobe, 5

freq: 10/15 ev: PCS

syndrome OMIM 610353

Epilepsy, Nocturnal Frontal Lobe, Type 4

syndrome OMIM 221820

Hereditary Diffuse Leukoencephalopathy With Spheroids

syndrome OMIM 236250

Homocystinuria Due To Deficiency of N(5,10)-Methylenetetrahydrofolate Reductase Activity

syndrome OMIM 615422

Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 2

freq: 1/5 ev: PCS

syndrome OMIM 617532

Intellectual Developmental Disorder With Neuropsychiatric Features

syndrome OMIM 304700

Jensen Syndrome

syndrome OMIM 300867

Kabuki Syndrome 2

syndrome OMIM 614257

Mental Retardation, Autosomal Dominant 11

freq: 5/10 ev: PCS

syndrome OMIM 616973

Mental Retardation, Autosomal Dominant 42

freq: 4/13 ev: PCS

disease OMIM 613970

Mental Retardation, Autosomal Dominant 6

freq: 6/6 ev: PCS

syndrome OMIM 136630

Mental Retardation, Fra12A Type

freq: 1/8 ev: PCS

syndrome OMIM 300958

Mental Retardation, X-Linked 102

freq: 1/5 ev: PCS

syndrome OMIM 300984

Mental Retardation, X-Linked 105

syndrome OMIM 300957

Mental Retardation, X-Linked 12

freq: 15/38 ev: PCS

syndrome OMIM 300114

Mental Retardation, X-Linked 15

freq: HP:0040283 ev: TAS

syndrome OMIM 300957

Mental Retardation, X-Linked 35

freq: 15/38 ev: PCS

syndrome OMIM 300114

Mental Retardation, X-Linked 49

freq: HP:0040283 ev: TAS

syndrome OMIM 300978

Mental Retardation, X-Linked 61

syndrome OMIM 300799

Mental Retardation, X-Linked, Syndromic, Raymond Type

freq: HP:0040283 ev: IEA

syndrome OMIM 304700

Mohr-Tranebjaerg Syndrome

syndrome OMIM 236250

Mthfr Deficiency, Thermolabile Type

syndrome OMIM 617114

Myopathy, Myofibrillar, 7

freq: 1/2 ev: PCS

syndrome OMIM 603472

Neuronal Intranuclear Inclusion Disease

freq: 12/56 ev: PCS

syndrome OMIM 309510

Partington X-Linked Mental Retardation Syndrome

freq: 8/28 ev: PCS