About: Iris hypoplasia with glaucoma

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

Iris hypoplasia with glaucoma, also known as Iris hypoplasia and glaucoma or simply IHG is a very rare genetic disorder which is characterized by a combination of an underdeveloped of the iris and glaucoma. It has been described in three families; two from Russia and one from London, U.K. It was mapped to a duplication of the q25 region of chromosome 6 through the London family. Tooth agenesis can sometimes be associated with this disorder.

Property	Value
dbo:abstract	Iris hypoplasia with glaucoma, also known as Iris hypoplasia and glaucoma or simply IHG is a very rare genetic disorder which is characterized by a combination of an underdeveloped of the iris and glaucoma. It has been described in three families; two from Russia and one from London, U.K. It was mapped to a duplication of the q25 region of chromosome 6 through the London family. Tooth agenesis can sometimes be associated with this disorder. (en)
dbo:alias	(en) Iris hypoplasia and glaucoma, IHG (en)
dbo:thumbnail	wiki-commons:Special:FilePath/Depiction_of_vision_for_a_Glaucoma_patient.png?width=300
dbo:wikiPageID	71006534 (xsd:integer)
dbo:wikiPageLength	3243 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID	1093446362 (xsd:integer)
dbo:wikiPageWikiLink	dbr:United_Kingdom dbc:Rare_genetic_syndromes dbr:Russia dbr:Genetic_mutation dbr:London dbr:Medical_genetics dbr:Glaucoma dbc:Genetic_diseases_and_disorders dbr:Chromosome_6 dbc:Rare_diseases dbc:Congenital_disorders_of_eyes dbr:Ophthalmology
dbp:causes	dbr:Genetic_mutation
dbp:deaths	- (en)
dbp:duration	Lifelong (en)
dbp:frequency	Rare, although 3 families have been described, there could be more, since iris hypoplasia and accompanying glaucoma can't be as rare as 3 families out of 2 billion (en)
dbp:onset	Conception (en)
dbp:prevention	None (en)
dbp:prognosis	Medium (en)
dbp:specialty	dbr:Medical_genetics dbr:Ophthalmology
dbp:symptoms	ocular anomalies (en)
dbp:synonyms	Iris hypoplasia and glaucoma, IHG (en)
dbp:wikiPageUsesTemplate	dbt:Reflist dbt:Ophthalmology-stub dbt:Infobox_medical_condition
dcterms:subject	dbc:Rare_genetic_syndromes dbc:Genetic_diseases_and_disorders dbc:Rare_diseases dbc:Congenital_disorders_of_eyes
rdf:type	owl:Thing wikidata:Q12136 dbo:Disease
rdfs:comment	Iris hypoplasia with glaucoma, also known as Iris hypoplasia and glaucoma or simply IHG is a very rare genetic disorder which is characterized by a combination of an underdeveloped of the iris and glaucoma. It has been described in three families; two from Russia and one from London, U.K. It was mapped to a duplication of the q25 region of chromosome 6 through the London family. Tooth agenesis can sometimes be associated with this disorder. (en)
rdfs:label	Iris hypoplasia with glaucoma (en)
owl:sameAs	wikidata:Iris hypoplasia with glaucoma https://global.dbpedia.org/id/Dchhg
prov:wasDerivedFrom	wikipedia-en:Iris_hypoplasia_with_glaucoma?oldid=1093446362&ns=0
foaf:depiction	wiki-commons:Special:FilePath/Depiction_of_vision_for_a_Glaucoma_patient.png
foaf:isPrimaryTopicOf	wikipedia-en:Iris_hypoplasia_with_glaucoma
is dbo:wikiPageWikiLink of	dbr:Axenfeld–Rieger_syndrome
is foaf:primaryTopic of	wikipedia-en:Iris_hypoplasia_with_glaucoma