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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 DISORDER OF CHILDHOOD ONSET;   CHROMOSOME 15q11-q13 DUPLICATION SYNDROME;   CHROMOSOME Xp22 DELETION SYNDROME;   Early Infantile Autism;   Epsilon-Trimethyllysine Hydroxylase Deficiency;   Kanner syndrome;   Kanner's syndrome;   Kanners syndrome;   TMLHED;   autism;   autism-related phrase speech delay;   autistic behavior;   autistic disorders;   childhood autism;   infantile autism
 narrow_synonym: ASD;   Autism 1;   Autism, Severe;   CHD8-RELATED DISORDERS;   CHROMOSOME 15q11.2 DUPLICATION SYNDROME;   X-linked mental retardation
 related_synonym: AUTISM, SUSCEPTIBILITY TO, 20;   AUTISTIC DISORDER AUTISM, SUSCEPTIBILITY TO, 1;   AUTS1;   AUTS10;   AUTS11;   AUTS12;   AUTS13;   AUTS15;   AUTS16;   AUTS17;   AUTS18;   AUTS19;   AUTS2;   AUTS20;   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, 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: 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:612100;   OMIM:613410;   OMIM:613436;   OMIM:615032;   OMIM:615091
 xref: ICD10CM:F84.0;   ICD9CM:299.0;   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 17638
    Developmental Diseases 11033
      Neurodevelopmental Disorders 5594
        Pervasive Child Development Disorders 2730
          autism spectrum disorder 2727
            autistic disorder 2549
              16p11.2 Deletion Syndrome 38
              Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies 1
              NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS 1
              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 17638
    disease of anatomical entity 16240
      nervous system disease 12501
        central nervous system disease 10583
          brain disease 9772
            disease of mental health 7306
              developmental disorder of mental health 4080
                pervasive developmental disorder 2733
                  autism spectrum disorder 2727
                    autistic disorder 2549
                      16p11.2 Deletion Syndrome 38
                      Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies 1
                      NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS 1
                      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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