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- Feingold_syndrome abstract "Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who first described the syndrome in 1975. Until 2003, at least 79 patients have been reported worldwide.".
- Feingold_syndrome diseasesdb "33706".
- Feingold_syndrome omim "164280".
- Feingold_syndrome thumbnail Autosomal_dominant_-_en.svg?width=300.
- Feingold_syndrome wikiPageExternalLink NBK7050.
- Feingold_syndrome wikiPageID "11574390".
- Feingold_syndrome wikiPageRevisionID "591294898".
- Feingold_syndrome diseasesdb "33706".
- Feingold_syndrome genereviewsname "Feingold Syndrome 1".
- Feingold_syndrome genereviewsnbk "NBK7050".
- Feingold_syndrome hasPhotoCollection Feingold_syndrome.
- Feingold_syndrome name "Feingold syndrome".
- Feingold_syndrome omim "164280".
- Feingold_syndrome wordnet_type synset-disease-noun-1.
- Feingold_syndrome subject Category:Autosomal_dominant_disorders.
- Feingold_syndrome subject Category:Syndromes.
- Feingold_syndrome subject Category:Transcription_factor_deficiencies.
- Feingold_syndrome type Abstraction100002137.
- Feingold_syndrome type Attribute100024264.
- Feingold_syndrome type AutosomalDominantDisease114162025.
- Feingold_syndrome type AutosomalDominantDisorders.
- Feingold_syndrome type Cognition100023271.
- Feingold_syndrome type Complex105870365.
- Feingold_syndrome type Concept105835747.
- Feingold_syndrome type Condition113920835.
- Feingold_syndrome type Content105809192.
- Feingold_syndrome type Disease114070360.
- Feingold_syndrome type GeneticDisease114151139.
- Feingold_syndrome type Idea105833840.
- Feingold_syndrome type IllHealth114052046.
- Feingold_syndrome type Illness114061805.
- Feingold_syndrome type Lack114449405.
- Feingold_syndrome type Need114449126.
- Feingold_syndrome type PathologicalState114051917.
- Feingold_syndrome type PhysicalCondition114034177.
- Feingold_syndrome type PsychologicalFeature100023100.
- Feingold_syndrome type State100024720.
- Feingold_syndrome type Syndrome105870790.
- Feingold_syndrome type Syndromes.
- Feingold_syndrome type TranscriptionFactorDeficiencies.
- Feingold_syndrome type Whole105869584.
- Feingold_syndrome type Disease.
- Feingold_syndrome type AilmentCondition.
- Feingold_syndrome type Situation.
- Feingold_syndrome comment "Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who first described the syndrome in 1975. Until 2003, at least 79 patients have been reported worldwide.".
- Feingold_syndrome label "Feingold syndrome".
- Feingold_syndrome label "Zespół Feingolda".
- Feingold_syndrome sameAs Zespół_Feingolda.
- Feingold_syndrome sameAs m.02rjqph.
- Feingold_syndrome sameAs Q5441566.
- Feingold_syndrome sameAs Q5441566.
- Feingold_syndrome sameAs 400.
- Feingold_syndrome sameAs Feingold_syndrome.
- Feingold_syndrome wasDerivedFrom Feingold_syndrome?oldid=591294898.
- Feingold_syndrome depiction Autosomal_dominant_-_en.svg.
- Feingold_syndrome isPrimaryTopicOf Feingold_syndrome.
- Feingold_syndrome name "Feingold syndrome".
