About: Katz syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Katz syndrome is a rare congenital disorder, presenting as a polymalformative syndrome characterized by enlarged viscera, hepatomegaly, diabetes, and skeletal anomalies that result in a short stature, cranial hyperostosis, and typical facial features. It is probably a variant of the autosomal recessive type of Craniometaphyseal Dysplasia.

Property	Value
dbo:abstract	Katz syndrome is a rare congenital disorder, presenting as a polymalformative syndrome characterized by enlarged viscera, hepatomegaly, diabetes, and skeletal anomalies that result in a short stature, cranial hyperostosis, and typical facial features. It is probably a variant of the autosomal recessive type of Craniometaphyseal Dysplasia. (en)
dbo:thumbnail	wiki-commons:Special:FilePath/Hyperostosis_frontalis_interna_-_Roe_seitlich.jpg?width=300
dbo:wikiPageID	35495758 (xsd:integer)
dbo:wikiPageLength	1873 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID	1053097282 (xsd:integer)
dbo:wikiPageWikiLink	dbr:Viscera dbc:Rare_genetic_syndromes dbc:Syndromes_with_craniofacial_abnormalities dbc:Syndromes_with_short_stature dbr:Syndrome dbr:Medical_genetics dbr:Autosomal dbr:Craniometaphyseal_Dysplasia_Autosomal_Dominant dbc:Congenital_disorders dbc:Rare_syndromes dbr:Hyperostosis dbc:Syndromes_affecting_the_hepatobiliary_system dbr:Hepatomegaly dbr:Diabetes dbr:Recessive dbr:Congenital_disorder
dbp:caption	Hyperostosis frontalis interna in a 74-year-old woman (en)
dbp:field	dbr:Medical_genetics
dbp:synonyms	Hyperostosis frontalis interna (en)
dbp:wikiPageUsesTemplate	dbt:Congenital-malformation-stub dbt:Citation_needed dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Reflist
dcterms:subject	dbc:Rare_genetic_syndromes dbc:Syndromes_with_craniofacial_abnormalities dbc:Syndromes_with_short_stature dbc:Congenital_disorders dbc:Rare_syndromes dbc:Syndromes_affecting_the_hepatobiliary_system
gold:hypernym	dbr:Disorder
rdf:type	owl:Thing wikidata:Q12136 yago:WikicatCongenitalDisorders yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:BirthDefect114465048 yago:Condition113920835 yago:Defect114464005 yago:Disease114070360 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 dbo:Disease yago:State100024720
rdfs:comment	Katz syndrome is a rare congenital disorder, presenting as a polymalformative syndrome characterized by enlarged viscera, hepatomegaly, diabetes, and skeletal anomalies that result in a short stature, cranial hyperostosis, and typical facial features. It is probably a variant of the autosomal recessive type of Craniometaphyseal Dysplasia. (en)
rdfs:label	Katz syndrome (en)
owl:sameAs	freebase:Katz syndrome yago-res:Katz syndrome wikidata:Katz syndrome https://global.dbpedia.org/id/4pA6s
prov:wasDerivedFrom	wikipedia-en:Katz_syndrome?oldid=1053097282&ns=0
foaf:depiction	wiki-commons:Special:FilePath/Hyperostosis_frontalis_interna_-_Roe_seitlich.jpg
foaf:isPrimaryTopicOf	wikipedia-en:Katz_syndrome
is dbo:wikiPageDisambiguates of	dbr:Katz
is dbo:wikiPageWikiLink of	dbr:List_of_congenital_disorders dbr:List_of_diseases_(K) dbr:List_of_syndromes dbr:Katz
is foaf:primaryTopic of	wikipedia-en:Katz_syndrome