Self-injurious behavior

Symptom Information:

Symptom ID: HPO:0100716
Synonyms:
Autoagression [HPO:0100716]
SELF-INJURIOUS BEHAVIORS [HPO:0100716]
Self-injurious behaviour [HPO:0100716]
Self mutilation [Orphanet:43640]
Self-harm (finding) [Orphanet:43640]
Self-mutilation (finding) [Orphanet:43640]
Self Mutilation [Orphanet:43640]
Self-harm [Orphanet:43640]
Self-injurious behavior [OMIM:Self-injurious behavior]
Self-injurious behaviors [OMIM:Self-injurious behaviors]
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]
Self injurious behavior [OMIM:Self injurious behavior]
Self-mutilation (if left untreated) [OMIM:Self-mutilation (if left untreated)]
Self injurious behaviour [MedDRA:10063495]
Self-abusive bahavior [IBIS,cm]
Quality:
Cross references:
HPO:0001218 "Autoamputation" [Orphanet:43640]
HPO:0000718 "Aggressive behavior" [Orphanet:43640]
HPO:0000742 "Self-mutilation" [Orphanet:43640]
Orphanet:43640 "Auto-aggressivity/auto-mutilation" [Orphanet:43640]
OMIM: "Self-injurious behavior" [OMIM:Self-injurious behavior]
OMIM: "Self-injurious behaviors" [OMIM:Self-injurious behaviors]
OMIM: "Self injurious behavior" [OMIM:Self injurious behavior]
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
MedDRA Suicidal and self-injurious behaviour
Orphanet Behavioral abnormality
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)
                         Self-injurious behavior(HPO:0100716)
MedDRA:
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microdeletion syndrome (Orphanet:261236)
17q12 microduplication syndrome (Orphanet:261272)
19p13.12 microdeletion syndrome (Orphanet:254346)
1p36 deletion syndrome (Orphanet:1606)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q37 microdeletion syndrome (Orphanet:1001)
4-hydroxybutyric aciduria (Orphanet:22)
4q21 microdeletion syndrome (Orphanet:238750)
Adenylosuccinate lyase deficiency (Orphanet:46)
Alexander disease (Orphanet:58)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
CHARGE syndrome (Orphanet:138)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
Choreoacanthocytosis (Orphanet:2388)
Classical phenylketonuria (Orphanet:79254)
Coffin-Lowry syndrome (Orphanet:192)
Congenital erythropoietic porphyria (Orphanet:79277)
Cornelia de Lange syndrome (Orphanet:199)
Distal monosomy 6p (Orphanet:96125)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Fragile X syndrome (Orphanet:908)
Gómez-López-Hernández syndrome (Orphanet:1532)
Harlequin ichthyosis (Orphanet:457)
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type (Orphanet:86923)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Keratoderma hereditarium mutilans (Orphanet:494)
Keratoderma hereditarium mutilans with ichthyosis (Orphanet:79395)
Kleefstra syndrome (Orphanet:261494)
Lesch-Nyhan syndrome (Orphanet:510)
Maternal hyperphenylalaninemia (Orphanet:2209)
Microphthalmia, Lenz type (Orphanet:568)
Norrie disease (Orphanet:649)
Oculocerebrorenal syndrome (Orphanet:534)
Phenylketonuria (Orphanet:716)
Rett syndrome (Orphanet:778)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Transketolase deficiency (ORPHA:488618)
Wolfram syndrome 2 (OMIM:604928)