×
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
Lysosomal Storage Diseases, Nervous System
A group of enzymatic disorders affecting the nervous system and to a variable degree the skeletal system, lymphoreticular system, and other organs. The conditions are marked by an abnormal accumulation of catabolic material within lysosomes.
推出的年份: 2000
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:
C10.228.140.163.100.435, C16.320.565.189.435, C16.320.565.595.554, C18.452.132.100.435, C18.452.648.189.435, C18.452.648.595.554
MeSH 单一 ID:
D020140
进入的组:
Lysosomal Enzyme Disorders, Nervous System
Nervous System Lysosomal Enzyme Disorders
Nervous System Lysosomal Storage Diseases
早前的内容:
Brain Diseases (1964-1999)
Lysosomal Storage Diseases (1992-1999)
Lysosomes (1964-1999)
Sphingolipidoses (1974-1999)
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Brain Diseases, Metabolic [C10.228.140.163]
Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
Adrenoleukodystrophy [C10.228.140.163.100.084]
Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
Galactosemias [C10.228.140.163.100.320]
Hartnup Disease [C10.228.140.163.100.355]
Hepatolenticular Degeneration [C10.228.140.163.100.360]
Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
add_circle
Homocystinuria [C10.228.140.163.100.365]
Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
Hyperlysinemias [C10.228.140.163.100.380]
Leigh Disease [C10.228.140.163.100.412]
Lesch-Nyhan Syndrome [C10.228.140.163.100.425]
Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
Fucosidosis [C10.228.140.163.100.435.295]
Glycogen Storage Disease Type II [C10.228.140.163.100.435.340]
Mucolipidoses [C10.228.140.163.100.435.590]
Sialic Acid Storage Disease [C10.228.140.163.100.435.810]
Sphingolipidoses [C10.228.140.163.100.435.825]
add_circle
Maple Syrup Urine Disease [C10.228.140.163.100.520]
MELAS Syndrome [C10.228.140.163.100.535]
Menkes Kinky Hair Syndrome [C10.228.140.163.100.540]
MERRF Syndrome [C10.228.140.163.100.545]
Mevalonate Kinase Deficiency [C10.228.140.163.100.593]
Oculocerebrorenal Syndrome [C10.228.140.163.100.640]
Phenylketonurias [C10.228.140.163.100.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C10.228.140.163.100.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C10.228.140.163.100.750]
Refsum Disease [C10.228.140.163.100.813]
Refsum Disease, Infantile [C10.228.140.163.100.844]
Tyrosinemias [C10.228.140.163.100.875]
Urea Cycle Disorders, Inborn [C10.228.140.163.100.937]
add_circle
Zellweger Syndrome [C10.228.140.163.100.968]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Adrenoleukodystrophy [C16.320.565.189.084]
Cerebral Amyloid Angiopathy, Familial [C16.320.565.189.168]
Galactosemias [C16.320.565.189.320]
Hartnup Disease [C16.320.565.189.355]
Hepatolenticular Degeneration [C16.320.565.189.360]
Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362]
add_circle
Homocystinuria [C16.320.565.189.365]
Hyperglycinemia, Nonketotic [C16.320.565.189.375]
Hyperlysinemias [C16.320.565.189.380]
Leigh Disease [C16.320.565.189.412]
Lesch-Nyhan Syndrome [C16.320.565.189.425]
Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
Fucosidosis [C16.320.565.189.435.295]
Glycogen Storage Disease Type II [C16.320.565.189.435.340]
Mucolipidoses [C16.320.565.189.435.590]
Sialic Acid Storage Disease [C16.320.565.189.435.810]
Sphingolipidoses [C16.320.565.189.435.825]
add_circle
Maple Syrup Urine Disease [C16.320.565.189.520]
MELAS Syndrome [C16.320.565.189.535]
Menkes Kinky Hair Syndrome [C16.320.565.189.540]
MERRF Syndrome [C16.320.565.189.545]
Mevalonate Kinase Deficiency [C16.320.565.189.593]
Oculocerebrorenal Syndrome [C16.320.565.189.640]
Phenylketonurias [C16.320.565.189.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C16.320.565.189.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C16.320.565.189.750]
Refsum Disease [C16.320.565.189.813]
Refsum Disease, Infantile [C16.320.565.189.844]
Tyrosinemias [C16.320.565.189.875]
Urea Cycle Disorders, Inborn [C16.320.565.189.937]
add_circle
Zellweger Syndrome [C16.320.565.189.968]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Lysosomal Storage Diseases [C16.320.565.595]
Aspartylglucosaminuria [C16.320.565.595.100]
Cholesterol Ester Storage Disease [C16.320.565.595.201]
add_circle
Cystinosis [C16.320.565.595.377]
Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
Fucosidosis [C16.320.565.595.554.295]
Glycogen Storage Disease Type II [C16.320.565.595.554.340]
Mucolipidoses [C16.320.565.595.554.590]
Sialic Acid Storage Disease [C16.320.565.595.554.810]
Sphingolipidoses [C16.320.565.595.554.825]
add_circle
Mannosidase Deficiency Diseases [C16.320.565.595.577]
add_circle
Mucopolysaccharidoses [C16.320.565.595.600]
add_circle
Pycnodysostosis [C16.320.565.595.800]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Brain Diseases, Metabolic [C18.452.132]
Brain Diseases, Metabolic, Inborn [C18.452.132.100]
Adrenoleukodystrophy [C18.452.132.100.084]
Cerebral Amyloid Angiopathy, Familial [C18.452.132.100.168]
Galactosemias [C18.452.132.100.320]
Hartnup Disease [C18.452.132.100.355]
Hepatolenticular Degeneration [C18.452.132.100.360]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362]
add_circle
Homocystinuria [C18.452.132.100.365]
Hyperglycinemia, Nonketotic [C18.452.132.100.375]
Hyperlysinemias [C18.452.132.100.380]
Leigh Disease [C18.452.132.100.412]
Lesch-Nyhan Syndrome [C18.452.132.100.425]
Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
Fucosidosis [C18.452.132.100.435.295]
Glycogen Storage Disease Type II [C18.452.132.100.435.340]
Mucolipidoses [C18.452.132.100.435.590]
Sialic Acid Storage Disease [C18.452.132.100.435.810]
Sphingolipidoses [C18.452.132.100.435.825]
add_circle
Maple Syrup Urine Disease [C18.452.132.100.520]
MELAS Syndrome [C18.452.132.100.535]
Menkes Kinky Hair Syndrome [C18.452.132.100.540]
MERRF Syndrome [C18.452.132.100.545]
Mevalonate Kinase Deficiency [C18.452.132.100.593]
Oculocerebrorenal Syndrome [C18.452.132.100.640]
Phenylketonurias [C18.452.132.100.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C18.452.132.100.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.132.100.750]
Refsum Disease [C18.452.132.100.813]
Refsum Disease, Infantile [C18.452.132.100.844]
Tyrosinemias [C18.452.132.100.875]
Urea Cycle Disorders, Inborn [C18.452.132.100.937]
add_circle
Zellweger Syndrome [C18.452.132.100.968]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Adrenoleukodystrophy [C18.452.648.189.084]
Cerebral Amyloid Angiopathy, Familial [C18.452.648.189.168]
Galactosemias [C18.452.648.189.320]
Hartnup Disease [C18.452.648.189.355]
Hepatolenticular Degeneration [C18.452.648.189.360]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362]
add_circle
Homocystinuria [C18.452.648.189.365]
Hyperglycinemia, Nonketotic [C18.452.648.189.375]
Hyperlysinemias [C18.452.648.189.380]
Leigh Disease [C18.452.648.189.412]
Lesch-Nyhan Syndrome [C18.452.648.189.425]
Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
Fucosidosis [C18.452.648.189.435.295]
Glycogen Storage Disease Type II [C18.452.648.189.435.340]
Mucolipidoses [C18.452.648.189.435.590]
Sialic Acid Storage Disease [C18.452.648.189.435.810]
Sphingolipidoses [C18.452.648.189.435.825]
add_circle
Maple Syrup Urine Disease [C18.452.648.189.520]
MELAS Syndrome [C18.452.648.189.535]
Menkes Kinky Hair Syndrome [C18.452.648.189.540]
MERRF Syndrome [C18.452.648.189.545]
Mevalonate Kinase Deficiency [C18.452.648.189.593]
Oculocerebrorenal Syndrome [C18.452.648.189.640]
Phenylketonurias [C18.452.648.189.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C18.452.648.189.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.648.189.750]
Refsum Disease [C18.452.648.189.813]
Refsum Disease, Infantile [C18.452.648.189.844]
Tyrosinemias [C18.452.648.189.875]
Urea Cycle Disorders, Inborn [C18.452.648.189.937]
add_circle
Zellweger Syndrome [C18.452.648.189.968]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Lysosomal Storage Diseases [C18.452.648.595]
Aspartylglucosaminuria [C18.452.648.595.100]
Cholesterol Ester Storage Disease [C18.452.648.595.201]
add_circle
Cystinosis [C18.452.648.595.377]
Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
Fucosidosis [C18.452.648.595.554.295]
Glycogen Storage Disease Type II [C18.452.648.595.554.340]
Mucolipidoses [C18.452.648.595.554.590]
Sialic Acid Storage Disease [C18.452.648.595.554.810]
Sphingolipidoses [C18.452.648.595.554.825]
add_circle
Mannosidase Deficiency Diseases [C18.452.648.595.577]
add_circle
Mucopolysaccharidoses [C18.452.648.595.600]
add_circle
Pycnodysostosis [C18.452.648.595.800]
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)