| Descriptor English: | Corneal Dystrophy, Juvenile Epithelial of Meesmann | ||||||
| Descriptor Spanish: |
Distrofia Corneal Epitelial Juvenil de Meesmann
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| Descriptor Portuguese: | Distrofia Corneana Epitelial Juvenil de Meesmann | ||||||
| Descriptor French: | Dystrophie cornéenne de Meesmann | ||||||
| Entry term(s): |
Corneal Dystrophies, Meesmann Corneal Dystrophy, Meesmann Corneal Dystrophy, Meesmann Epithelial Dystrophies, Meesmann Corneal Juvenile Hereditary Epithelial Dystrophy Meesmann Corneal Dystrophies Meesmann Corneal Dystrophy Meesmann Corneal Epithelial Dystrophy Meesmann Epithelial Corneal Dystrophy |
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| Tree number(s): |
C11.204.236.218 C11.270.162.218 C16.320.290.162.204 |
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| RDF Unique Identifier: | https://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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Cornea (1954-1964) Corneal Dystrophies, Hereditary (1965-2006) |
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| Public MeSH Note: | 2007 |
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| History Note: | 2007 |
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| DeCS ID: | 52116 | ||||||
| Unique ID: | D053559 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2007/01/01 | ||||||
| Date of Entry: | 2006/07/05 | ||||||
| Revision Date: | 2013/07/08 |
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DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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Corneal Dystrophy, Juvenile Epithelial of Meesmann
- Preferred
| Concept UI |
M0494580 |
| 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. |
| Preferred term | Corneal Dystrophy, Juvenile Epithelial of Meesmann |
| Entry term(s) |
Corneal Dystrophies, Meesmann Corneal Dystrophy, Meesmann Corneal Dystrophy, Meesmann Epithelial Dystrophies, Meesmann Corneal Juvenile Hereditary Epithelial Dystrophy Meesmann Corneal Dystrophies Meesmann Corneal Dystrophy Meesmann Corneal Epithelial Dystrophy Meesmann Epithelial Corneal Dystrophy |
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