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ONTOLOGY REPORT - ANNOTATIONS


Term:Feingold syndrome
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Accession:DOID:0060464 term browser browse the term
Definition:An autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (DO)
Synonyms:exact_synonym: BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY;   Brunner Winter syndrome;   Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum;   FGLDS;   MMT syndrome;   MODED;   MODED syndrome;   Microcephaly and Digital Abnormalities with Normal Intelligence;   Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome;   Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula (MMT) Syndrome;   Microcephaly-Oculo-Digito-Esophageal-Duodenal (MODED) Syndrome;   Microcephaly-oculo-digito-esophageal-duodenal syndrome;   ODED;   ODED syndrome;   Oculo-Digito-Esophagoduodental (ODED) Syndrome;   Oculodigitoesophagoduodenal Syndrome;   microcephaly-digital anomalies-normal intelligence syndrome;   oculo-digito-esophageal-duodenal syndrome
 primary_id: MESH:C537734
 alt_id: RDO:0003627
 xref: GARD:8407;   ORDO:1305
For additional species annotation, visit the Alliance of Genome Resources.


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Feingold syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mycn MYCN proto-oncogene, bHLH transcription factor JBrowse link 6 38,222,554 38,228,419 RGD:8554872
RGD:11554173
Feingold Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mycn MYCN proto-oncogene, bHLH transcription factor JBrowse link 6 38,222,554 38,228,419 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Feingold syndrome 1
        Feingold Syndrome 1 1
        Feingold Syndrome 2 0
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            disease of mental health 4314
              developmental disorder of mental health 2584
                specific developmental disorder 1319
                  intellectual disability 1146
                    Feingold syndrome 1
                      Feingold Syndrome 1 1
                      Feingold Syndrome 2 0
paths to the root