Search on: CORNEAL DYSTROPHY, JUVENILE EPITHELIAL OF MEESMANN 
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Descriptor English:   Corneal Dystrophy, Juvenile Epithelial of Meesmann 
Descriptor Spanish:   Distrofia Corneal Epitelial Juvenil de Meesmann 
Descriptor Portuguese:   Distrofia Corneana Epitelial Juvenil de Meesmann 
Synonyms English:   Corneal Dystrophy, Meesmann
Corneal Dystrophy, Meesmann Epithelial
Juvenile Hereditary Epithelial Dystrophy
Meesmann Corneal Dystrophy
Meesmann Corneal Epithelial Dystrophy
Meesmann Epithelial Corneal Dystrophy
Corneal Dystrophies, Meesmann
Dystrophies, Meesmann Corneal
Meesmann Corneal Dystrophies  
Tree Number:   C11.204.236.218
C11.270.162.218
C16.320.290.162.204
Definition English:   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. 
History Note English:   2007 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   52116 
Unique Identifier:   D053559 

Occurrence in VHL:
 

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