×
Close
註冊
登入
主页
用户
博客
照片
视频
医学图书S馆
医学图书M馆
医学图书D馆
医学术语
群组
活动
用户工具
用户指南
问答
谁看过我
反馈
语言
English
中文
推广
所有
MeSH descriptor
Mesh Subheading
Mesh Supplementary Concept
Mesh Pharmacological Action
search
搜索
清除所有
MeSH 搜索器
AND
OR
加入MeSH搜索引擎
搜索PubMed论文列
清除所有
Lipid Metabolism, Inborn Errors
Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.
推出的年份: 1965
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C16.320.565.398, C18.452.584.563, C18.452.648.398
MeSH 单一 ID:
D008052
进入的组:
Lipid Metabolism, Inborn Error
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
add_circle
Amino Acid Transport Disorders, Inborn [C16.320.565.151]
add_circle
Amyloidosis, Familial [C16.320.565.176]
add_circle
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
add_circle
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
add_circle
Cytochrome-c Oxidase Deficiency [C16.320.565.240]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
add_circle
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Barth Syndrome [C16.320.565.398.224]
Hyperlipidemia, Familial Combined [C16.320.565.398.450]
Hyperlipoproteinemia Type I [C16.320.565.398.465]
Hyperlipoproteinemia Type II [C16.320.565.398.481]
add_circle
Hyperlipoproteinemia Type III [C16.320.565.398.483]
Hyperlipoproteinemia Type IV [C16.320.565.398.487]
Hyperlipoproteinemia Type V [C16.320.565.398.493]
Hypolipoproteinemias [C16.320.565.398.500]
add_circle
Lipidoses [C16.320.565.398.641]
add_circle
Lipodystrophy, Congenital Generalized [C16.320.565.398.745]
Smith-Lemli-Opitz Syndrome [C16.320.565.398.850]
Xanthomatosis, Cerebrotendinous [C16.320.565.398.925]
Lysosomal Storage Diseases [C16.320.565.595]
add_circle
Metal Metabolism, Inborn Errors [C16.320.565.618]
add_circle
Peroxisomal Disorders [C16.320.565.663]
add_circle
Progeria [C16.320.565.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
add_circle
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Steroid Metabolism, Inborn Errors [C16.320.565.925]
add_circle
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Lipid Metabolism Disorders [C18.452.584]
Dyslipidemias [C18.452.584.500]
add_circle
Lipid Metabolism, Inborn Errors [C18.452.584.563]
Barth Syndrome [C18.452.584.563.224]
Hyperlipidemia, Familial Combined [C18.452.584.563.450]
Hyperlipoproteinemia Type I [C18.452.584.563.465]
Hyperlipoproteinemia Type II [C18.452.584.563.481]
add_circle
Hyperlipoproteinemia Type III [C18.452.584.563.483]
Hyperlipoproteinemia Type IV [C18.452.584.563.487]
Hyperlipoproteinemia Type V [C18.452.584.563.493]
Hypobetalipoproteinemia, Familial, Apolipoprotein B [C18.452.584.563.497]
Hypolipoproteinemias [C18.452.584.563.500]
add_circle
Lipidoses [C18.452.584.563.641]
add_circle
Lipodystrophy, Congenital Generalized [C18.452.584.563.745]
Lipodystrophy, Familial Partial [C18.452.584.563.798]
Shwachman-Diamond Syndrome [C18.452.584.563.824]
Smith-Lemli-Opitz Syndrome [C18.452.584.563.850]
Xanthomatosis, Cerebrotendinous [C18.452.584.563.925]
Lipodystrophy [C18.452.584.625]
add_circle
Lipomatosis [C18.452.584.718]
add_circle
Xanthomatosis [C18.452.584.750]
add_circle
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
add_circle
Amino Acid Transport Disorders, Inborn [C18.452.648.151]
add_circle
Amyloidosis, Familial [C18.452.648.176]
add_circle
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
add_circle
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
add_circle
Hyperbilirubinemia, Hereditary [C18.452.648.300]
add_circle
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Barth Syndrome [C18.452.648.398.224]
Hyperlipidemia, Familial Combined [C18.452.648.398.450]
Hyperlipoproteinemia Type I [C18.452.648.398.465]
Hyperlipoproteinemia Type II [C18.452.648.398.481]
add_circle
Hyperlipoproteinemia Type III [C18.452.648.398.483]
Hyperlipoproteinemia Type IV [C18.452.648.398.487]
Hyperlipoproteinemia Type V [C18.452.648.398.493]
Hypolipoproteinemias [C18.452.648.398.500]
add_circle
Lipidoses [C18.452.648.398.641]
add_circle
Lipodystrophy, Congenital Generalized [C18.452.648.398.745]
Smith-Lemli-Opitz Syndrome [C18.452.648.398.850]
Xanthomatosis, Cerebrotendinous [C18.452.648.398.925]
Lysosomal Storage Diseases [C18.452.648.595]
add_circle
Metal Metabolism, Inborn Errors [C18.452.648.618]
add_circle
Peroxisomal Disorders [C18.452.648.663]
add_circle
Progeria [C18.452.648.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C18.452.648.798]
add_circle
Renal Tubular Transport, Inborn Errors [C18.452.648.893]
Steroid Metabolism, Inborn Errors [C18.452.648.925]
add_circle
thumb_up
Like
share
分享
favorite
书签
0
0
0
0
0
0
0
留言 (
0
)
gif
登入或註冊以發表你的留言
Modal title
×
Modal title
×
分享
登入
Global News and Health Forum
Join Now!
馬上登入
記住我
忘記密碼?
或者使用
Linkedin
留言 (0)