FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Feingold syndrome ID (Ontology) DOID:0060464 (Human Disease)
Definition A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.
Also Known As "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum" ; "FGLDS" ; "microcephaly-digital anomalies-normal intelligence syndrome" (for all, see Synonyms field below)
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 Genes
 Feingold syndrome       1
 for disease ribbon | Feingold syndrome       1
 model of | Feingold syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Feingold syndrome  1 rec.
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Is a autosomal dominant disease
syndrome
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Synonyms
  • "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum" EXACT
    "FGLDS" EXACT OMO:0003012
    "microcephaly-digital anomalies-normal intelligence syndrome" EXACT
    "microcephaly-oculo-digito-esophageal-duodenal syndrome" EXACT
    "MODED syndrome" EXACT
    "oculo-digito-esophageal-duodenal syndrome" EXACT
    "ODED syndrome" EXACT
Secondary IDs
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GARD:8407
ICD10CM:Q87.8
MESH:C537734
MIM:164280
MIM:614326
ORDO:1305