Autoamputation

Symptom Information:

Symptom ID: HPO:0001218
Synonyms:
Self mutilation [Orphanet:43640]
Self-harm (finding) [Orphanet:43640]
Self-mutilation (finding) [Orphanet:43640]
Self Mutilation [Orphanet:43640]
Self-harm [Orphanet:43640]
Autoamputation [OMIM:Autoamputation]
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:0100716 "Autoagression" [Orphanet:43640]
HPO:0000718 "Aggressive behavior" [Orphanet:43640]
HPO:0000742 "Self-mutilation" [Orphanet:43640]
Orphanet:43640 "Auto-aggressivity/auto-mutilation" [Orphanet:43640]
OMIM: "Autoamputation" [OMIM:Autoamputation]
OMIM: "Self-mutilation (if left untreated)" [OMIM:Self-mutilation (if left untreated)]
UMLS:C1833222 "Autoamputation" [HPO:0001218]
UMLS:C0036601 "Self Mutilation" [Orphanet:43640]
UMLS:C0424366 "Self-harm" [Orphanet:43640]
Is a (Direct Parents):
MedDRA Suicidal and self-injurious behaviour
Orphanet Behavioral abnormality
HPO         Abnormality of limb bone morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Autoamputation(HPO:0001218)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Classical phenylketonuria (Orphanet:79254)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Keratoderma hereditarium mutilans (Orphanet:494)
Maternal hyperphenylalaninemia (Orphanet:2209)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA (OMIM:162400)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)
Phenylketonuria (Orphanet:716)