Feingold Syndrome 1 (FGLDS1)

Alias:
Feingold Syndrome
Oculodigitoesophagoduodenal Syndrome
Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum
Oded Syndrome
Microcephaly-Digital Anomalies-Normal Intelligence Syndrome
Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome
Oculo-Digito-Esophageal-Duodenal Syndrome
Feingold Syndrome Type 1
Brunner-Winter Syndrome
Moded Syndrome
Mmt Syndrome
Fglds1
Fglds
Microcephaly-Intellectual Disability-Tracheoesophageal Fistula Syndrome
Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome Syndrome
Moded
Oded
Mmt
Fs
Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum Type 1
Microcephaly-Intellectual Disability-Tracheoesophageal Fistula Syndrome Type 1
Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome
Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome Syndrome Type 1
Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula Syndrome
Microcephaly-Digital Anomalies-Normal Intelligence Syndrome Type 1
Microcephaly Mesobrachyphalangy Tracheoesophageal Fistula Syndrome
Microcephaly and Digital Abnormalities with Normal Intelligence
Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome
Oculo-Digito-Esophageal-Duodenal Syndrome Type 1
Oculo-Digito-Esophagoduodental Syndrome
Brunner-Winter Syndrome Type 1
Feingold Syndrome, Type 1
Moded Syndrome Type 1
Oded Syndrome Type 1
Mmt Type 1
Fs1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Feingold Syndrome 1, also known as feingold syndrome, is related to esophageal atresia and anus, imperforate. An important gene associated with Feingold Syndrome 1 is MYCN (MYCN Proto-Oncogene, BHLH Transcription Factor), and among its related pathways/superpathways are miRNAs involved in DNA damage response and miRNA role in immune response in sepsis. Affiliated tissues include small intestine and bone, and related phenotypes are microcephaly and brachydactyly
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
12
196
38

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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