Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Schmitt_Gillenwater_Kelly_syndrome> ?p ?o. }
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- Schmitt_Gillenwater_Kelly_syndrome abstract "Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant congenital disorder consisting of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.".
- Schmitt_Gillenwater_Kelly_syndrome omim "179250".
- Schmitt_Gillenwater_Kelly_syndrome thumbnail Autosomal_dominant_-_en.svg?width=300.
- Schmitt_Gillenwater_Kelly_syndrome wikiPageID "422525".
- Schmitt_Gillenwater_Kelly_syndrome wikiPageRevisionID "561477942".
- Schmitt_Gillenwater_Kelly_syndrome hasPhotoCollection Schmitt_Gillenwater_Kelly_syndrome.
- Schmitt_Gillenwater_Kelly_syndrome name "Schmitt Gillenwater Kelly syndrome".
- Schmitt_Gillenwater_Kelly_syndrome omim "179250".
- Schmitt_Gillenwater_Kelly_syndrome wordnet_type synset-disease-noun-1.
- Schmitt_Gillenwater_Kelly_syndrome subject Category:Autosomal_dominant_disorders.
- Schmitt_Gillenwater_Kelly_syndrome subject Category:Congenital_disorders_of_musculoskeletal_system.
- Schmitt_Gillenwater_Kelly_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Schmitt_Gillenwater_Kelly_syndrome subject Category:Rare_diseases.
- Schmitt_Gillenwater_Kelly_syndrome subject Category:Syndromes.
- Schmitt_Gillenwater_Kelly_syndrome type Abnormality114501726.
- Schmitt_Gillenwater_Kelly_syndrome type Abstraction100002137.
- Schmitt_Gillenwater_Kelly_syndrome type Anomaly114505821.
- Schmitt_Gillenwater_Kelly_syndrome type Attribute100024264.
- Schmitt_Gillenwater_Kelly_syndrome type AutosomalDominantDisease114162025.
- Schmitt_Gillenwater_Kelly_syndrome type AutosomalDominantDisorders.
- Schmitt_Gillenwater_Kelly_syndrome type BirthDefect114465048.
- Schmitt_Gillenwater_Kelly_syndrome type Cognition100023271.
- Schmitt_Gillenwater_Kelly_syndrome type Complex105870365.
- Schmitt_Gillenwater_Kelly_syndrome type Concept105835747.
- Schmitt_Gillenwater_Kelly_syndrome type Condition113920835.
- Schmitt_Gillenwater_Kelly_syndrome type CongenitalDisordersOfMusculoskeletalSystem.
- Schmitt_Gillenwater_Kelly_syndrome type Content105809192.
- Schmitt_Gillenwater_Kelly_syndrome type Defect114464005.
- Schmitt_Gillenwater_Kelly_syndrome type Disease114070360.
- Schmitt_Gillenwater_Kelly_syndrome type GeneticDisease114151139.
- Schmitt_Gillenwater_Kelly_syndrome type GeneticDisordersWithOMIMButNoGene.
- Schmitt_Gillenwater_Kelly_syndrome type Idea105833840.
- Schmitt_Gillenwater_Kelly_syndrome type IllHealth114052046.
- Schmitt_Gillenwater_Kelly_syndrome type Illness114061805.
- Schmitt_Gillenwater_Kelly_syndrome type Imperfection114462666.
- Schmitt_Gillenwater_Kelly_syndrome type PathologicalState114051917.
- Schmitt_Gillenwater_Kelly_syndrome type PhysicalCondition114034177.
- Schmitt_Gillenwater_Kelly_syndrome type PsychologicalFeature100023100.
- Schmitt_Gillenwater_Kelly_syndrome type State100024720.
- Schmitt_Gillenwater_Kelly_syndrome type Syndrome105870790.
- Schmitt_Gillenwater_Kelly_syndrome type Syndromes.
- Schmitt_Gillenwater_Kelly_syndrome type Whole105869584.
- Schmitt_Gillenwater_Kelly_syndrome type Disease.
- Schmitt_Gillenwater_Kelly_syndrome type AilmentCondition.
- Schmitt_Gillenwater_Kelly_syndrome type Situation.
- Schmitt_Gillenwater_Kelly_syndrome comment "Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant congenital disorder consisting of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.".
- Schmitt_Gillenwater_Kelly_syndrome label "Schmitt Gillenwater Kelly syndrome".
- Schmitt_Gillenwater_Kelly_syndrome sameAs m.026mdd.
- Schmitt_Gillenwater_Kelly_syndrome sameAs Q7431830.
- Schmitt_Gillenwater_Kelly_syndrome sameAs Q7431830.
- Schmitt_Gillenwater_Kelly_syndrome sameAs Schmitt_Gillenwater_Kelly_syndrome.
- Schmitt_Gillenwater_Kelly_syndrome wasDerivedFrom Schmitt_Gillenwater_Kelly_syndrome?oldid=561477942.
- Schmitt_Gillenwater_Kelly_syndrome depiction Autosomal_dominant_-_en.svg.
- Schmitt_Gillenwater_Kelly_syndrome isPrimaryTopicOf Schmitt_Gillenwater_Kelly_syndrome.
- Schmitt_Gillenwater_Kelly_syndrome name "Schmitt Gillenwater Kelly syndrome".