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ONTOLOGY REPORT - ANNOTATIONS


Term:Feingold syndrome
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Accession:DOID:0060464 term browser browse the term
Definition:A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (DO)
Synonyms:exact_synonym: Brunner Winter syndrome;   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;   brachydactyly with short stature and microcephaly;   digital anomalies with short palpebral fissures and atresia of esophagus or duodenum;   microcephaly-digital anomalies-normal intelligence syndrome;   oculo-digito-esophageal-duodenal syndrome;   oculo-digito-esophagoduodental (ODED) syndrome;   oculodigitoesophagoduodenal syndrome
 primary_id: MESH:C537734
 xref: GARD:8407;   OMIM:PS164280;   ORDO:1305
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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: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 16021
    syndrome 6144
      Feingold syndrome 1
        Feingold Syndrome 1 1
        Feingold Syndrome 2 0
Path 2
Term Annotations click to browse term
  disease 16021
    Developmental Diseases 9337
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8165
        genetic disease 7689
          monogenic disease 5447
            autosomal genetic disease 4411
              autosomal dominant disease 2754
                complex cortical dysplasia with other brain malformations 528
                  Malformations of Cortical Development, Group I 378
                    microcephaly 222
                      Feingold syndrome 1
                        Feingold Syndrome 1 1
                        Feingold Syndrome 2 0
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