Self-mutilation

Symptom Information:

Symptom ID: HPO:0000742
Synonyms:
Self mutilation [HPO:0000742]
Self mutilation [Orphanet:43640]
Self-harm (finding) [Orphanet:43640]
Self-mutilation (finding) [Orphanet:43640]
self-mutilation [HPO:0000742]
Self Mutilation [Orphanet:43640]
Self-harm [Orphanet:43640]
Self mutilation [OMIM:Self mutilation]
Self-mutilation [OMIM:Self-mutilation]
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-mutilation (if left untreated) [OMIM:Self-mutilation (if left untreated)]
Quality:
Cross references:
HPO:0001218 "Autoamputation" [Orphanet:43640]
HPO:0100716 "Autoagression" [Orphanet:43640]
HPO:0000718 "Aggressive behavior" [Orphanet:43640]
Orphanet:43640 "Auto-aggressivity/auto-mutilation" [Orphanet:43640]
OMIM: "Self mutilation" [OMIM:Self mutilation]
OMIM: "Self-mutilation" [OMIM:Self-mutilation]
OMIM: "Self-mutilation (if left untreated)" [OMIM:Self-mutilation (if left untreated)]
UMLS:C2242914 "self-mutilation" [HPO:0000742]
UMLS:C0036601 "Self Mutilation" [Orphanet:43640]
UMLS:C0424366 "Self-harm" [Orphanet:43640]
Is a (Direct Parents):
MedDRA Suicidal and self-injurious behaviour
HPO         Self-injurious behavior
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)
                            Self-mutilation(HPO:0000742)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Adenylosuccinate lyase deficiency (Orphanet:46)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Classical phenylketonuria (Orphanet:79254)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
GILLES DE LA TOURETTE SYNDROME (OMIM:137580)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hereditary sensory and autonomic neuropathy type 5 (Orphanet:64752)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 20 (OMIM:614970)
LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT (OMIM:308950)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48 (OMIM:616269)
MGAT2-CDG (Orphanet:79329)
MICROHYDRANENCEPHALY (OMIM:605013)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Maternal hyperphenylalaninemia (Orphanet:2209)
Monosomy 5p (Orphanet:281)
Navajo neurohepatopathy (Orphanet:255229)
Phenylketonuria (Orphanet:716)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Tyrosinemia type 1 (Orphanet:882)
Tyrosinemia type 2 (Orphanet:28378)