Autistic behavior

Symptom Information:

Symptom ID: HPO:0000729
Synonyms:
AUTISM SPECTRUM DISORDERS [HPO:0000729]
Pervasive developmental disorder [HPO:0000729]
Autism spectrum disorder [OMIM:Autism spectrum disorder]
Autism spectrum disorders [OMIM:Autism spectrum disorders]
Pervasive developmental disorder [OMIM:Pervasive developmental disorder]
Autism spectrum disorder (in some patients) [OMIM:Autism spectrum disorder (in some patients)]
Autism spectrum disorder (less common) [OMIM:Autism spectrum disorder (less common)]
Autism spectrum disorder (rare) [OMIM:Autism spectrum disorder (rare)]
Developmental disorder, pervasive [OMIM:Developmental disorder, pervasive]
Pervasive developmental disorder (CVS+) [OMIM:Pervasive developmental disorder (CVS+)]
Autism spectrum disorder [MedDRA:10063844]
Autistic features [OMIM,du]
Quality:
Cross references:
OMIM: "Autism spectrum disorder" [OMIM:Autism spectrum disorder]
OMIM: "Autism spectrum disorders" [OMIM:Autism spectrum disorders]
OMIM: "Pervasive developmental disorder" [OMIM:Pervasive developmental disorder]
OMIM: "Autism spectrum disorder (in some patients)" [OMIM:Autism spectrum disorder (in some patients)]
OMIM: "Autism spectrum disorder (less common)" [OMIM:Autism spectrum disorder (less common)]
OMIM: "Autism spectrum disorder (rare)" [OMIM:Autism spectrum disorder (rare)]
OMIM: "Developmental disorder, pervasive" [OMIM:Developmental disorder, pervasive]
OMIM: "Pervasive developmental disorder (CVS+)" [OMIM:Pervasive developmental disorder (CVS+)]
Is a (Direct Parents):
HPO         Abnormal emotion/affect behavior
MedDRA Pervasive developmental disorders NEC
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:
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)