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ONTOLOGY REPORT - ANNOTATIONS


Term:autistic disorder
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Accession:DOID:12849 term browser browse the term
Definition:A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V)
Synonyms:exact_synonym: AUTISM WITH OR WITHOUT SEIZURES;   AUTISTIC BEHAVIOR;   AUTISTIC DISORDER OF CHILDHOOD ONSET;   CHROMOSOME 15q11-q13 DUPLICATION SYNDROME;   CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB;   CHROMOSOME Xp22 DELETION SYNDROME;   Disorders, Autistic;   Early Infantile Autism;   Epsilon-Trimethyllysine Hydroxylase Deficiency;   Infantile Autism;   Kanner syndrome;   Kanner's Syndrome;   Kanners Syndrome;   PHRASE SPEECH DELAY, AUTISM-RELATED;   TMLHED;   autism;   childhood autism
 narrow_synonym: ASD;   Autism 1;   Autism, Severe;   CHD8-RELATED DISORDERS;   CHROMOSOME 15q11.2 DUPLICATION SYNDROME;   mental retardation, X-linked
 related_synonym: AUTISTIC DISORDER AUTISM, SUSCEPTIBILITY TO, 1;   AUTS1;   AUTS10;   AUTS11;   AUTS12;   AUTS13;   AUTS14A;   AUTS15;   AUTS16;   AUTS17;   AUTS18;   AUTS19;   AUTS2;   AUTS3;   AUTS4;   AUTS5;   AUTS7;   AUTS8;   AUTS9;   AUTSX1;   AUTSX2;   AUTSX3;   AUTSX4;   AUTSX5;   AUTSX6;   Autism, Susceptibility to, X-Linked 1;   Autism, Susceptibility to, X-Linked 2;   Autism, Susceptibility to, X-Linked 3;   Autism, Susceptibility to, X-Linked 4;   Autism, Susceptibility to, X-Linked 5;   Autism, Susceptibility to, X-Linked 6;   Autism-Speech Delay;   DUPLICATION 15q11-q13 SYNDROME AUTISM, SUSCEPTIBILITY TO, 4;   autism, susceptibility to, 10;   autism, susceptibility to, 11;   autism, susceptibility to, 12;   autism, susceptibility to, 13;   autism, susceptibility to, 14A;   autism, susceptibility to, 15;   autism, susceptibility to, 16;   autism, susceptibility to, 17;   autism, susceptibility to, 18;   autism, susceptibility to, 3;   autism, susceptibility to, 5;   autism, susceptibility to, 7;   autism, susceptibility to, 8;   autism, susceptibility to, 9;   autism, susceptibility to,19
 primary_id: MESH:D001321
 alt_id: DOID:9000370;   DOID:9001692;   DOID:9002442;   DOID:9003751;   DOID:9007719;   OMIM:209850;   OMIM:300425;   OMIM:300495;   OMIM:300496;   OMIM:300830;   OMIM:300847;   OMIM:300872;   OMIM:606053;   OMIM:607373;   OMIM:608049;   OMIM:608636;   OMIM:609378;   OMIM:610676;   OMIM:610836;   OMIM:610838;   OMIM:610908;   OMIM:611015;   OMIM:611016;   OMIM:611913;   OMIM:612100;   OMIM:613410;   OMIM:613436;   OMIM:615032;   OMIM:615091;   RDO:0004948;   RDO:0008591;   RDO:0008602;   RDO:0008603;   RDO:9000297;   RDO:9000410;   RDO:9001133
 xref: NCI:C97161;   OMIM:PS209850;   ORDO:106
For additional species annotation, visit the Alliance of Genome Resources.


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Path 1
Term Annotations click to browse term
  disease 16432
    Developmental Diseases 10215
      Neurodevelopmental Disorders 5271
        Pervasive Child Development Disorders 2646
          autism spectrum disorder 2643
            autistic disorder 2474
              16p11.2 Deletion Syndrome 28
              Timothy syndrome 3
              adenylosuccinase lyase deficiency 1
              branched-chain keto acid dehydrogenase kinase deficiency 40
              chromosome 1q21.1 duplication syndrome 0
              intellectual disability-severe speech delay-mild dysmorphism syndrome 1
              macrocephaly-autism syndrome 2
Path 2
Term Annotations click to browse term
  disease 16432
    disease of anatomical entity 15407
      nervous system disease 11675
        central nervous system disease 9550
          brain disease 8971
            disease of mental health 6910
              developmental disorder of mental health 3789
                pervasive developmental disorder 2649
                  autism spectrum disorder 2643
                    autistic disorder 2474
                      16p11.2 Deletion Syndrome 28
                      Timothy syndrome 3
                      adenylosuccinase lyase deficiency 1
                      branched-chain keto acid dehydrogenase kinase deficiency 40
                      chromosome 1q21.1 duplication syndrome 0
                      intellectual disability-severe speech delay-mild dysmorphism syndrome 1
                      macrocephaly-autism syndrome 2
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