serw-MX  [xml]  
 


    
 Categorias DeCS

A09 Sense Organs .
A09.371 Eye 3998 .
A09.371.894 Uvea 11169 .
A09.371.894.223 Choroid .
C11 Eye Diseases .
C11.250 Eye Abnormalities .
C11.250.110 Coloboma .
C11.270 Eye Diseases, Hereditary .
C11.270.468 Gyrate Atrophy .
C11.941 Uveal Diseases .
C11.941.160 Choroid Diseases .
C11.941.160.578 Gyrate Atrophy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.384 Eye Abnormalities .
C16.131.384.282 Coloboma .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.468 Gyrate Atrophy .
G01 Physical Phenomena .
G01.590 Optical Phenomena .
G01.590.310 Iridescence .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Coloboma .
Coloboma Of Iris, Choroid, And Retina .
Coloboma, Ocular .
Coloboma, Uveoretinal .
Ocular Coloboma .
Uveoretinal Coloboma .
Colobomas .
1.00
 
Gyrate Atrophy .
Gyrate Atrophy of Choroid and Retina .
Gyrate Atrophy of the Choroid and Retina .
Hyperornithinemia with Gyrate Atrophy of Choroid and Retina .
OAT Deficiency .
OKT Deficiency .
Ornithine Aminotransferase Deficiency .
Ornithine Keto Acid Aminotransferase Deficiency .
Ornithine Ketoacid Aminotransferase Deficiency .
Ornithine-Delta-Aminotransferase Deficiency .
Ornithinemia with Gyrate Atrophy .
Atrophy, Gyrate .
Deficiency, OAT .
Deficiency, OKT .
Deficiency, Ornithine Aminotransferase .
Deficiency, Ornithine-Delta-Aminotransferase .
Ornithine Delta Aminotransferase Deficiency .
0.55
 
Choroid .
Choroids .
0.43
 
Iridescence .
Goniochromism .
Iridescent Coloring .
Opalescence .
Pearlescence .
Coloring, Iridescent .
Colorings, Iridescent .
Iridescent Colorings .
0.39