Behavioral abnormality
Symptom Information:
Symptom ID: | HPO:0000708 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |