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中文Lattice Corneal Dystrophy
Alias:
Familial Amyloid Neuropathy, Finnish Type
Familial Amyloid Polyneuropathy, Type V
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晶状体角膜营养不良，又称家族性淀粉样神经病，芬兰型，与角膜营养不良，晶状体型I和角膜营养不良，胶状滴状有关。与晶状体角膜营养不良有关的重要基因是TGFBI（转化生长因子β诱导），其相关通路/超级通路包括Ca，cAMP和脂质信号传导和雄激素受体活性的共调节。附属组织包括眼睛和肾脏，相关表型包括增加SMN2外显子7的包含和稳态/代谢
Related ID：
MESH：C537935
Basic Information
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MALACARDS
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MGI
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