×
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
Acatalasia
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.
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:
C16.320.565.663.050, C18.452.648.663.050
MeSH 单一 ID:
D020642
进入的组:
Takahara Disease
Disease, Takahara
Takahara's Disease
Disease, Takahara's
Takaharas Disease
Acatalasemia
Hypocatalasemia
Hypocatalasia
Catalase Deficiency
Catalase Deficiencies
Deficiencies, Catalase
Deficiency, Catalase
Acatalasemia Japanese Type
Japanese Type, Acatalasemia
Acatalasemia Swiss Type
Swiss Type, Acatalasemia
早前的内容:
Catalase (1965-1999)
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Peroxisomal Disorders [C16.320.565.663]
Acatalasia [C16.320.565.663.050]
Adrenoleukodystrophy [C16.320.565.663.100]
Chondrodysplasia Punctata, Rhizomelic [C16.320.565.663.265]
Mevalonate Kinase Deficiency [C16.320.565.663.430]
Refsum Disease [C16.320.565.663.760]
Refsum Disease, Infantile [C16.320.565.663.865]
Zellweger Syndrome [C16.320.565.663.970]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Peroxisomal Disorders [C18.452.648.663]
Acatalasia [C18.452.648.663.050]
Adrenoleukodystrophy [C18.452.648.663.100]
Chondrodysplasia Punctata, Rhizomelic [C18.452.648.663.265]
Mevalonate Kinase Deficiency [C18.452.648.663.430]
Refsum Disease [C18.452.648.663.760]
Refsum Disease, Infantile [C18.452.648.663.865]
Zellweger Syndrome [C18.452.648.663.970]
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)