Aggressive behavior
Symptom Information:
Symptom ID: | HPO:0000718 | |||||||||||||||||||||||||||
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) Abnormal emotion/affect behavior(HPO:0100851) Abnormal aggressive, impulsive or violent behavior(HPO:0006919) Aggressive behavior(HPO:0000718) MedDRA: |
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Database Frequency: | 109 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
1p36 deletion syndrome | (Orphanet:1606) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3q29 microdeletion syndrome | (Orphanet:65286) |
4-hydroxybutyric aciduria | (Orphanet:22) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
Beta-mannosidosis | (Orphanet:118) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
CHROMOSOME Xp22 DELETION SYNDROME | (OMIM:300830) |
CK syndrome | (Orphanet:251383) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Choreoacanthocytosis | (Orphanet:2388) |
Citrullinemia type II | (Orphanet:247585) |
Classical phenylketonuria | (Orphanet:79254) |
Coffin-Siris syndrome | (Orphanet:1465) |
DPAGT1-CDG | (Orphanet:86309) |
Developmental delay with autism spectrum disorder and gait instability | (Orphanet:329195) |
Distal monosomy 10q | (Orphanet:96148) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 2 | (OMIM:603204) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 | (OMIM:615005) |
FRAXE intellectual deficit | (Orphanet:100973) |
Familial long QT syndrome | (Orphanet:768) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
GILLES DE LA TOURETTE SYNDROME | (OMIM:137580) |
Gaucher disease type 3 | (Orphanet:77261) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Glycine encephalopathy | (Orphanet:407) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Huntington disease-like 1 | (Orphanet:157941) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperprolinemia type 1 | (Orphanet:419) |
Hypertryptophanemia | (Orphanet:2224) |
Intellectual deficiency - hypotonia - spasticity - sleep disorder | (Orphanet:356996) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Jawad syndrome | (Orphanet:313795) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 20 | (OMIM:614970) |
Kleefstra syndrome | (Orphanet:261494) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Lesch-Nyhan syndrome | (Orphanet:510) |
Lipoid proteinosis | (Orphanet:530) |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES | (OMIM:613670) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 | (OMIM:615828) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 30 | (OMIM:616083) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | (OMIM:614202) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27 | (OMIM:614340) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 | (OMIM:615541) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 | (OMIM:616116) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48 | (OMIM:616269) |
MENTAL RETARDATION, X-LINKED 30 | (OMIM:300558) |
MENTAL RETARDATION, X-LINKED 99 | (OMIM:300919) |
MGAT2-CDG | (Orphanet:79329) |
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:604321) |
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:614852) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 | (OMIM:615824) |
MONOAMINE OXIDASE A | (OMIM:309850) |
Marden-Walker syndrome | (Orphanet:2461) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 5p | (Orphanet:281) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Nasu-Hakola disease | (Orphanet:2770) |
Norrie disease | (Orphanet:649) |
Obesity due to leptin receptor gene deficiency | (Orphanet:179494) |
Oculocerebrorenal syndrome | (Orphanet:534) |
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL | (OMIM:612691) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Phenylketonuria | (Orphanet:716) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Richards-Rundle syndrome | (Orphanet:1399) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Sneddon syndrome | (Orphanet:820) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Urocanic aciduria | (Orphanet:210128) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked epilepsy - learning disabilities - behavior disorders | (Orphanet:85294) |
X-linked intellectual disability due to GRIA3 anomalies | (Orphanet:364028) |
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome | (Orphanet:85295) |