Autistic behavior
Symptom Information:
Symptom ID: | HPO:0000729 | ||||||||||||
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) Autistic behavior(HPO:0000729) MedDRA: |
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Database Frequency: | 27 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
46,XY SEX REVERSAL 9 | (OMIM:616067) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Alström syndrome | (Orphanet:64) |
Autism spectrum disorder-epilepsy-arthrogryposis syndrome | (Orphanet:370943) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
CHROMOSOME 15q11.2 DELETION SYNDROME | (OMIM:615656) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
CHROMOSOME Xp22 DELETION SYNDROME | (OMIM:300830) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Christianson syndrome | (Orphanet:85278) |
Coffin-Siris syndrome | (Orphanet:1465) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
Familial focal epilepsy with variable foci | (Orphanet:98820) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HYPERLEXIA | (OMIM:238350) |
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome | (Orphanet:363611) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 5 | (OMIM:612621) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Rett syndrome | (Orphanet:778) |
SPECIFIC LANGUAGE IMPAIRMENT 5 | (OMIM:615432) |
Timothy syndrome | (Orphanet:65283) |
X-linked epilepsy - learning disabilities - behavior disorders | (Orphanet:85294) |