| 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 |
