MeSH Browser

MeSH Heading: Corneal Dystrophy, Juvenile Epithelial of Meesmann
Tree Number(s): C11.204.236.218; C11.270.162.218; C16.320.290.162.204
Unique ID: D053559
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D053559
Scope Note: An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.
Entry Term(s): Corneal Dystrophy, Meesmann; Corneal Dystrophy, Meesmann Epithelial; Juvenile Hereditary Epithelial Dystrophy; Meesmann Corneal Dystrophy; Meesmann Corneal Epithelial Dystrophy; Meesmann Epithelial Corneal Dystrophy
Previous Indexing: Cornea (1954-1964); Corneal Dystrophies, Hereditary (1965-2006)
Public MeSH Note: 2007
History Note: 2007
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Corneal Dystrophy, Juvenile Epithelial of Meesmann MeSH Descriptor Data 2024