Self-injurious behavior
Symptom Information:
Symptom ID: | HPO:0100716 | ||||||||||||||||||||||
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) Self-injurious behavior(HPO:0100716) MedDRA: |
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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) |