Behavioral abnormality

Symptom Information:

Symptom ID: HPO:0000708
Synonyms:
Behavioral changes [HPO:0000708]
Behavioral disorders [HPO:0000708]
Behavioral disturbances [HPO:0000708]
Behavioral problems [HPO:0000708]
Behavioral symptoms [HPO:0000708]
Behavioral/psychiatric abnormalities [HPO:0000708]
Psychiatric disorders [HPO:0000708]
Psychiatric disturbances [HPO:0000708]
Mental disorder [Orphanet:43560]
Behavior disorder [Orphanet:43560]
Mental disorder (disorder) [Orphanet:43560]
Mental disorders [Orphanet:43560]
Psychic disease [Orphanet:43560]
Behavior Disorders [Orphanet:43560]
Behavioral changes [OMIM:Behavioral changes]
Behavioral disorders [OMIM:Behavioral disorders]
Behavioral disturbances [OMIM:Behavioral disturbances]
Behavioral problems [OMIM:Behavioral problems]
Behavioral/psychiatric abnormalities [OMIM:Behavioral/psychiatric abnormalities]
Psychiatric disorders [OMIM:Psychiatric disorders]
Psychiatric disturbances [OMIM:Psychiatric disturbances]
Psychic/behavioural troubles [Orphanet:43560]
Psychic disturbance [Orphanet:43560]
Disorder behavior [Orphanet:43560]
Mental disorder [MedDRA:10061284]
Breakdown nervous [MedDRA:10061284]
Mental aberration [MedDRA:10061284]
Mental abnormality acute transient [MedDRA:10061284]
Mental disorder NOS [MedDRA:10061284]
Mental disorder transient [MedDRA:10061284]
Mental disorders complicating pregnancy, childbirth, or the puerperium [MedDRA:10061284]
Mental disorders of mother [MedDRA:10061284]
Mental disorders of mother, antepartum [MedDRA:10061284]
Mental disorders of mother, comp pregnancy, childbirth, or the puerp, unspec as to eoc [MedDRA:10061284]
Mental disorders of mother, complicating pregnancy, childbirth, or the puerperium, unspecified as to [MedDRA:10061284]
Mental disorders of mother, postpartum [MedDRA:10061284]
Mental disorders of mother, with delivery [MedDRA:10061284]
Mental disorders of mother, with delivery, with mention of postpartum complication [MedDRA:10061284]
Mental state abnormal [MedDRA:10061284]
Nervous breakdown [MedDRA:10061284]
Other and unspecified special symptoms or syndromes, not elsewhere classified [MedDRA:10061284]
Other specified drug-induced mental disorder [MedDRA:10061284]
Other specified drug-induced mental disorders [MedDRA:10061284]
Other specified psychophysiological malfunction [MedDRA:10061284]
Other specified transient organic mental disorder [MedDRA:10061284]
Other specified transient organic mental disorders [MedDRA:10061284]
Psychiatric disorder NOS [MedDRA:10061284]
Psychic disorder [MedDRA:10061284]
Psychic disorder NOS [MedDRA:10061284]
Psychic disturbance [MedDRA:10061284]
Psychic factors associated with diseases classified elsewhere [MedDRA:10061284]
Psychoneuropathy NOS [MedDRA:10061284]
Separation anxiety disorder [MedDRA:10061284]
Special symptoms or syndromes, not elsewhere classified [MedDRA:10061284]
Unspecified drug-induced mental disorder [MedDRA:10061284]
Unspecified psychophysiological malfunction [MedDRA:10061284]
Mental state abnormal aggravated [MedDRA:10061284]
Psychological disorder NOS [MedDRA:10061284]
Mental dysequilibrium [MedDRA:10061284]
Abnormal behavior [MedDRA:10061422]
Abnormal behavior NOS [MedDRA:10061422]
Behavior abnormal [MedDRA:10061422]
Behavior disorder [MedDRA:10061422]
Behaviour abnormal [MedDRA:10061422]
Behaviour disorder [MedDRA:10061422]
Behavioural disorder [MedDRA:10061422]
Bizarre behavior [MedDRA:10061422]
Disorder behavior [MedDRA:10061422]
Hallucination-like abnormal behavior [MedDRA:10061422]
Personal irresponsibility [MedDRA:10061422]
Vermiculation [MedDRA:10061422]
Bizarre behavior [MedDRA:10061422]
Hallucination-like abnormal behavior [MedDRA:10061422]
Behavioral disorders (rare) [OMIM:Behavioral disorders (rare)]
Behavioral disturbances (in some patients) [OMIM:Behavioral disturbances (in some patients)]
Behavioral disturbances (in some) [OMIM:Behavioral disturbances (in some)]
Psychiatric disturbances (25%) [OMIM:Psychiatric disturbances (25%)]
Psychiatric disturbances (9% of patients) [OMIM:Psychiatric disturbances (9% of patients)]
Psychiatric disorders [MedDRA:10037175]
Neurobehavioral changes associated with hyperammonemia [IBIS,cm]
Psychotic behavior [IBIS,cm]
Quality:
Cross references:
Orphanet:43560 "Psychic/behavioural troubles" [Orphanet:43560]
OMIM: "Behavioral changes" [OMIM:Behavioral changes]
OMIM: "Behavioral disorders" [OMIM:Behavioral disorders]
OMIM: "Behavioral disturbances" [OMIM:Behavioral disturbances]
OMIM: "Behavioral problems" [OMIM:Behavioral problems]
OMIM: "Behavioral/psychiatric abnormalities" [OMIM:Behavioral/psychiatric abnormalities]
OMIM: "Psychiatric disorders" [OMIM:Psychiatric disorders]
OMIM: "Psychiatric disturbances" [OMIM:Psychiatric disturbances]
OMIM: "Behavioral disorders (rare)" [OMIM:Behavioral disorders (rare)]
OMIM: "Behavioral disturbances (in some patients)" [OMIM:Behavioral disturbances (in some patients)]
OMIM: "Behavioral disturbances (in some)" [OMIM:Behavioral disturbances (in some)]
OMIM: "Psychiatric disturbances (25%)" [OMIM:Psychiatric disturbances (25%)]
OMIM: "Psychiatric disturbances (9% of patients)" [OMIM:Psychiatric disturbances (9% of patients)]
UMLS:C0004936 "Mental disorders" [Orphanet:43560]
UMLS:C0277577 "Psychic disease" [Orphanet:43560]
UMLS:C0004930 "Behavior Disorders" [Orphanet:43560]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
HPO         Abnormality of higher mental function
HPO         Abnormal consumption behavior
HPO         Perseveration
HPO         Abnormal drinking behavior
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)
MedDRA:
Database Frequency: 212 / 7739
Resource:

All diseases associated with this symptom:

15q11q13 microduplication syndrome (Orphanet:238446)
15q13.3 microdeletion syndrome (Orphanet:199318)
16p11.2p12.2 microduplication syndrome (Orphanet:261204)
16p13.11 microdeletion syndrome (Orphanet:261236)
16p13.11 microduplication syndrome (Orphanet:261243)
16p13.3 microduplication syndrome (Orphanet:96078)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 deletion syndrome (Orphanet:567)
2q37 microdeletion syndrome (Orphanet:1001)
4-hydroxybutyric aciduria (Orphanet:22)
48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
5q35 microduplication syndrome (Orphanet:228415)
8q22.1 microdeletion syndrome (Orphanet:178303)
ALZHEIMER DISEASE 3 (OMIM:607822)
Aarskog-Scott syndrome (Orphanet:915)
Aceruloplasminemia (Orphanet:48818)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acute intermittent porphyria (Orphanet:79276)
Adiposis dolorosa (Orphanet:36397)
Adrenomyeloneuropathy (Orphanet:139399)
Adult neuronal ceroid lipofuscinosis (Orphanet:79262)
Adult polyglucosan body disease (Orphanet:206583)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Alpha-mannosidosis (Orphanet:61)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Angelman syndrome (Orphanet:72)
Aniridia (Orphanet:77)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Aspartylglucosaminuria (Orphanet:93)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant cerebellar ataxia (Orphanet:99)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant nocturnal frontal lobe epilepsy (Orphanet:98784)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BREATH-HOLDING SPELLS (OMIM:607578)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Behçet disease (Orphanet:117)
CADASIL (Orphanet:136)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE, DISTAMYCIN A TYPE, RARE, FRA(16)(p12.1), INCLUDED (OMIM:136570)
CLN3 disease (Orphanet:228346)
CLN4A disease (Orphanet:228340)
CLN4B disease (Orphanet:228343)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Cerebellar ataxia - hypogonadism (Orphanet:1173)
Cerebroretinal vasculopathy (Orphanet:3421)
Cerebrotendinous xanthomatosis (Orphanet:909)
Choreoacanthocytosis (Orphanet:2388)
Christianson syndrome (Orphanet:85278)
Citrullinemia type I (Orphanet:247525)
Citrullinemia type II (Orphanet:247585)
Classical homocystinuria (Orphanet:394)
Classical phenylketonuria (Orphanet:79254)
Cornelia de Lange syndrome (Orphanet:199)
Cystinosis (Orphanet:213)
Diencephalic syndrome (Orphanet:1672)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 7q11.23 microduplication syndrome (Orphanet:261102)
Duchenne muscular dystrophy (Orphanet:98896)
Dwarfism - intellectual deficit - eye abnormality (Orphanet:2650)
Dyschondrosteosis - nephritis (Orphanet:1765)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 2 (OMIM:603204)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 4 (OMIM:610353)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 (OMIM:615005)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24 (OMIM:615871)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Fabry disease (Orphanet:324)
Familial atrial myxoma (Orphanet:615)
Familial dysautonomia (Orphanet:1764)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Fetal alcohol syndrome (Orphanet:1915)
Fragile X syndrome (Orphanet:908)
Fried syndrome (Orphanet:85335)
HERNS syndrome (Orphanet:63261)
Hereditary cerebral hemorrhage with amyloidosis, Arctic type (Orphanet:324723)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Hereditary cerebral hemorrhage with amyloidosis, Iowa type (Orphanet:324708)
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type (Orphanet:324703)
Hereditary coproporphyria (Orphanet:79273)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hereditary vascular retinopathy (Orphanet:71291)
Histidinemia (Orphanet:2157)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency (Orphanet:395)
Homocystinuria without methylmalonic aciduria (Orphanet:622)
Huntington disease (Orphanet:399)
Hurler syndrome (Orphanet:93473)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperinsulinism-hyperammonemia syndrome (Orphanet:35878)
Hyperlysinemia, type I (OMIM:238700)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypophosphatasia (Orphanet:436)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 2 (OMIM:615422)
Infantile Refsum disease (Orphanet:772)
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior (Orphanet:85329)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Intellectual deficit, X-linked, Cantagrel type (Orphanet:85277)
Intellectual deficit, X-linked, Raymond type (Orphanet:163953)
Isolated cerebellar hypoplasia/agenesis (Orphanet:1398)
Jacobsen syndrome (Orphanet:2308)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
KABUKI SYNDROME 2 (OMIM:300867)
Keipert syndrome (Orphanet:2662)
Kleefstra syndrome (Orphanet:261494)
Krabbe disease (Orphanet:487)
L-2-hydroxyglutaric aciduria (Orphanet:79314)
Leber plus disease (Orphanet:99718)
Lesch-Nyhan syndrome (Orphanet:510)
Locked-in syndrome (Orphanet:2406)
Lyme disease (Orphanet:91546)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 (OMIM:613970)
MENTAL RETARDATION, X-LINKED 90 (OMIM:300850)
MERRF (Orphanet:551)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Menkes disease (Orphanet:565)
Metachromatic leukodystrophy (Orphanet:512)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblD (Orphanet:79283)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
Microcephaly - seizures - developmental delay (Orphanet:228418)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mixed connective tissue disease (Orphanet:809)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Monilethrix (Orphanet:573)
Monoamine oxidase A deficiency (Orphanet:3057)
Monosomy 22q13 (Orphanet:48652)
Mucolipidosis type 4 (Orphanet:578)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Myhre syndrome (Orphanet:2588)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Nance-Horan syndrome (Orphanet:627)
Narcolepsy without cataplexy (Orphanet:83465)
Nasu-Hakola disease (Orphanet:2770)
Neuhauser-Eichner-Opitz syndrome (Orphanet:2672)
Neurocutaneous melanocytosis (Orphanet:2481)
Neuronal ceroid lipofuscinosis (Orphanet:216)
Neuronal intranuclear inclusion disease (Orphanet:2289)
Niemann-Pick disease type C (Orphanet:646)
Nipah virus disease (Orphanet:99825)
Non-polyposis Turcot syndrome (Orphanet:99817)
Norrie disease (Orphanet:649)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Ornithine transcarbamylase deficiency (Orphanet:664)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
Pallister-Hall syndrome (Orphanet:672)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Pelizaeus-Merzbacher disease (Orphanet:702)
Perry syndrome (Orphanet:178509)
Polyarteritis nodosa (Orphanet:767)
Porphyria (Orphanet:738)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Prader-Willi syndrome (Orphanet:739)
Progressive epilepsy-intellectual deficit, Finnish type (Orphanet:1947)
Propionic acidemia (Orphanet:35)
Proximal 16p11.2 microdeletion syndrome (Orphanet:261197)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Rabies (Orphanet:770)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Rett syndrome (Orphanet:778)
Rheumatic fever (Orphanet:3099)
SOTOS SYNDROME 1 (OMIM:117550)
Scleroderma (Orphanet:801)
Scrub typhus (Orphanet:83317)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Smith-Magenis syndrome (Orphanet:819)
Sneddon syndrome (Orphanet:820)
Sotos syndrome (Orphanet:821)
Steinert myotonic dystrophy (Orphanet:273)
Sturge-Weber syndrome (Orphanet:3205)
Symptomatic form of Coffin-Lowry syndrome in female carriers (Orphanet:276630)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
TRAPS syndrome (Orphanet:32960)
Testotoxicosis (Orphanet:3000)
Tuberous sclerosis (Orphanet:805)
Tyrosinemia type 2 (Orphanet:28378)
Tyrosinemia type 3 (Orphanet:69723)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 2 (Orphanet:231178)
Usher syndrome type 3 (Orphanet:231183)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Wyburn-Mason syndrome (Orphanet:53719)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
X-linked epilepsy - learning disabilities - behavior disorders (Orphanet:85294)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome (Orphanet:85295)