Aggressive behavior

Symptom Information:

Symptom ID: HPO:0000718
Synonyms:
Aggression [HPO:0000718]
Aggressive behaviour [HPO:0000718]
Aggressiveness [HPO:0000718]
Self mutilation [Orphanet:43640]
Self-harm (finding) [Orphanet:43640]
Self-mutilation (finding) [Orphanet:43640]
Self Mutilation [Orphanet:43640]
Self-harm [Orphanet:43640]
Aggression [OMIM:Aggression]
Aggressive behavior [OMIM:Aggressive behavior]
Aggressiveness [OMIM:Aggressiveness]
Auto-aggressivity/auto-mutilation [Orphanet:43640]
Intentional self-injury [MedDRA:10022524]
Deliberate self-harm [MedDRA:10022524]
Deliberate self-injury [MedDRA:10022524]
Parasuicide [MedDRA:10022524]
Repeated parasuicide [MedDRA:10022524]
Self mutilation [MedDRA:10022524]
Self inflicted laceration [MedDRA:10022524]
Aggression (if left untreated) [OMIM:Aggression (if left untreated)]
Aggression (in some patients) [OMIM:Aggression (in some patients)]
Aggressive behavior (2 patients) [OMIM:Aggressive behavior (2 patients)]
Aggressive behavior (in 1 family) [OMIM:Aggressive behavior (in 1 family)]
Aggressive behavior (in some patients) [OMIM:Aggressive behavior (in some patients)]
Self-mutilation (if left untreated) [OMIM:Self-mutilation (if left untreated)]
Aggression [MedDRA:10001488]
combativeness [IBIS,cm]
Quality:
Cross references:
HPO:0001218 "Autoamputation" [Orphanet:43640]
HPO:0100716 "Autoagression" [Orphanet:43640]
HPO:0000742 "Self-mutilation" [Orphanet:43640]
Orphanet:43640 "Auto-aggressivity/auto-mutilation" [Orphanet:43640]
OMIM: "Aggression" [OMIM:Aggression]
OMIM: "Aggressive behavior" [OMIM:Aggressive behavior]
OMIM: "Aggressiveness" [OMIM:Aggressiveness]
OMIM: "Aggression (if left untreated)" [OMIM:Aggression (if left untreated)]
OMIM: "Aggression (in some patients)" [OMIM:Aggression (in some patients)]
OMIM: "Aggressive behavior (2 patients)" [OMIM:Aggressive behavior (2 patients)]
OMIM: "Aggressive behavior (in 1 family)" [OMIM:Aggressive behavior (in 1 family)]
OMIM: "Aggressive behavior (in some patients)" [OMIM:Aggressive behavior (in some patients)]
OMIM: "Self-mutilation (if left untreated)" [OMIM:Self-mutilation (if left untreated)]
UMLS:C0036601 "Self Mutilation" [Orphanet:43640]
UMLS:C0424366 "Self-harm" [Orphanet:43640]
Is a (Direct Parents):
HPO         Abnormal aggressive, impulsive or violent behavior
Orphanet Behavioral abnormality
MedDRA Suicidal and self-injurious behaviour
MedDRA Behaviour and socialisation disturbances
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:
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)