About: Schmitt Gillenwater Kelly syndrome

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About: Schmitt Gillenwater Kelly syndrome Goto Sponge NotDistinct Permalink

An Entity of Type : yago:WikicatSyndromes, within Data Space : dbpedia.org associated with source document(s)

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http://dbpedia.org/describe/?url=http%3A%2F%2Fdbpedia.org%2Fresource%2FSchmitt_Gillenwater_Kelly_syndrome&graph=http%3A%2F%2Fdbpedia.org&graph=http%3A%2F%2Fdbpedia.org

Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant congenital disorder consisting of , triphalangeal thumbs, hypospadias, and maxillary diastema.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalDominantDisorders yago:WikicatCongenitalDisordersOfMusculoskeletalSystem yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:AutosomalDominantDisease114162025 yago:BirthDefect114465048 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Defect114464005 yago:Disease114070360 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisordersWithOMIMButNoGene disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes
rdfs:label	Schmitt Gillenwater Kelly syndrome (en)
rdfs:comment	Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant congenital disorder consisting of , triphalangeal thumbs, hypospadias, and maxillary diastema. (en)
foaf:name	Schmitt Gillenwater Kelly syndrome (en)
name	Schmitt Gillenwater Kelly syndrome (en)
foaf:depiction
dcterms:subject	Rare diseases Syndromes Congenital disorders of musculoskeletal system Genetic disorders with OMIM but no gene Autosomal dominant disorders
Wikipage page ID	422525 (xsd:integer)
Wikipage revision ID	1090155779 (xsd:integer)
Link from a Wikipage to another Wikipage	Hypospadias Phalanges Inheritance Rare diseases Teeth Syndromes Congenital disorders of musculoskeletal system Genetic disorders with OMIM but no gene Autosomal dominant disorders Jaw Thumb Dominance (genetics) Autosome Congenital abnormality dbr:Radial_hypoplasia
sameAs	Schmitt Gillenwater Kelly syndrome Schmitt Gillenwater Kelly syndrome Schmitt Gillenwater Kelly syndrome Schmitt Gillenwater Kelly syndrome
dbp:wikiPageUsesTemplate	dbt:Genetic-disorder-stub dbt:Clear dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Congenital_malformations_and_deformations_of_musculoskeletal_system
thumbnail	wiki-commons:Special:FilePath/Autosomal_dominant_-_en.svg?width=300
ICD	Q87.2 (en)
OMIM	179250 (xsd:integer)
Orphanet	2252 (xsd:integer)
caption	Schmitt Gillenwater Kelly syndrome has an autosomal dominant pattern of inheritance. (en)
image size	150 (xsd:integer)
synonyms	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome (en)
has abstract	Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant congenital disorder consisting of , triphalangeal thumbs, hypospadias, and maxillary diastema. (en)
gold:hypernym	Disorder
dbp:wordnet_type	http://www.w3.org/2006/03/wn/wn20/instances/synset-disease-noun-1
prov:wasDerivedFrom	wikipedia-en:Schmitt_Gillenwater_Kelly_syndrome?oldid=1090155779&ns=0
page length (characters) of wiki page	2118 (xsd:nonNegativeInteger)
ICD10	Q87.2
OMIM id	179250 (xsd:integer)
ORPHA	2252
foaf:isPrimaryTopicOf	wikipedia-en:Schmitt_Gillenwater_Kelly_syndrome
is Link from a Wikipage to another Wikipage of	List of diseases (S) Gillenwater Schmitt List of syndromes Schmitt gillenwater kelly syndrome
is Wikipage redirect of	Schmitt gillenwater kelly syndrome
is Wikipage disambiguates of	Gillenwater Schmitt
is foaf:primaryTopic of	wikipedia-en:Schmitt_Gillenwater_Kelly_syndrome

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