About: Meesmann Corneal Dystrophy

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About: Meesmann Corneal Dystrophy Goto Sponge Distinct Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Meesmann Corneal Dystrophy
rdfs:subClassOf	Corneal Dystrophies, Hereditary Rare Non-Neoplastic Disorder
Semantic_Type	Disease or Syndrome
Preferred_Name	Meesmann Corneal Dystrophy
UMLS_CUI	C0339277
FULL_SYN	Meesmann Corneal DystrophyPTNCI Juvenile Epithelial of Meesmann Corneal DystrophySYNCI
DEFINITION	An autosomal dominant inherited corneal disorder caused by mutations in the KRT3 and KRT12 genes. It is characterized by the formation of multiple tiny cysts in the epithelial layer of the cornea. The cysts may rupture, causing pain, redness and light sensitivity. Vision usually is not affected.NCI
code	C84795
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0494580
is sameAs of	Corneal Dystrophy, Juvenile Epithelial of Meesmann

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