×
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
Chromosome Aberrations
Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.
推出的年份: 1968
副标题
chemically induced
classification
drug effects
embryology
radiation effects
statistics and numerical data
veterinary
树号:
C23.550.210, G05.365.590.175
MeSH 单一 ID:
D002869
进入的组:
Aberration, Chromosome
Aberrations, Chromosome
Chromosome Aberration
Abnormalities, Chromosome
Abnormality, Chromosome
Chromosome Abnormality
Cytogenetic Abnormalities
Abnormalities, Cytogenetic
Abnormality, Cytogenetic
Cytogenetic Abnormality
Chromosome Abnormalities
Cytogenetic Aberrations
Aberration, Cytogenetic
Aberrations, Cytogenetic
Cytogenetic Aberration
Abnormalities, Chromosomal
Abnormality, Chromosomal
Chromosomal Abnormalities
Chromosomal Abnormality
Chromosomal Aberrations
Aberration, Chromosomal
Aberrations, Chromosomal
Chromosomal Aberration
Autosome Abnormalities
Abnormality, Autosome
Autosome Abnormality
Abnormalities, Autosome
早前的内容:
Chromosome Abnormalities (1966-1967)
All MeSH Categories
Diseases Category
Pathological Conditions, Signs and Symptoms [C23]
Pathologic Processes [C23.550]
Acantholysis [C23.550.035]
Arrhythmias, Cardiac [C23.550.073]
add_circle
Ascites [C23.550.081]
Atrial Remodeling [C23.550.113]
Azotemia [C23.550.145]
Cardiotoxicity [C23.550.161]
Channelopathies [C23.550.177]
Chromosome Aberrations [C23.550.210]
Abnormal Karyotype [C23.550.210.024]
add_circle
Aneuploidy [C23.550.210.050]
add_circle
Chromosomal Instability [C23.550.210.110]
add_circle
Chromosome Breakage [C23.550.210.170]
Chromosome Duplication [C23.550.210.182]
add_circle
Chromosome Inversion [C23.550.210.190]
Chromothripsis [C23.550.210.310]
Isochromosomes [C23.550.210.430]
Micronuclei, Chromosome-Defective [C23.550.210.570]
Nondisjunction, Genetic [C23.550.210.645]
add_circle
Polyploidy [C23.550.210.702]
add_circle
Ring Chromosomes [C23.550.210.760]
Sex Chromosome Aberrations [C23.550.210.815]
add_circle
Translocation, Genetic [C23.550.210.870]
add_circle
Death [C23.550.260]
add_circle
Dehydration [C23.550.274]
Delayed Graft Function [C23.550.277]
Disease [C23.550.288]
add_circle
Disease Attributes [C23.550.291]
add_circle
Dysbiosis [C23.550.308]
Emphysema [C23.550.325]
add_circle
Extravasation of Diagnostic and Therapeutic Materials [C23.550.340]
add_circle
Femoracetabular Impingement [C23.550.347]
Fibrosis [C23.550.355]
add_circle
Frailty [C23.550.359]
Genomic Instability [C23.550.362]
add_circle
Gliosis [C23.550.369]
Granuloma [C23.550.382]
add_circle
Granulomatosis, Orofacial [C23.550.384]
Growth Disorders [C23.550.393]
add_circle
Hemolysis [C23.550.403]
Hemorrhage [C23.550.414]
add_circle
Hyperammonemia [C23.550.421]
Hyperamylasemia [C23.550.425]
Hyperbilirubinemia [C23.550.429]
add_circle
Hyperplasia [C23.550.444]
Hyperuricemia [C23.550.449]
Hypovolemia [C23.550.455]
Inflammation [C23.550.470]
add_circle
Intraoperative Complications [C23.550.505]
add_circle
Ischemia [C23.550.513]
add_circle
Leukoaraiosis [C23.550.522]
Leukocytosis [C23.550.526]
Lithiasis [C23.550.537]
Long Term Adverse Effects [C23.550.543]
Malacoplakia [C23.550.548]
Menstruation Disturbances [C23.550.568]
add_circle
Metaplasia [C23.550.589]
add_circle
Muscle Weakness [C23.550.695]
Myotoxicity [C23.550.706]
Necrosis [C23.550.717]
add_circle
Neointima [C23.550.722]
Neoplastic Processes [C23.550.727]
add_circle
Nerve Degeneration [C23.550.737]
add_circle
Ochronosis [C23.550.744]
Ossification, Heterotopic [C23.550.751]
add_circle
Ototoxicity [C23.550.753]
Pigmentation Disorders [C23.550.755]
Polydipsia [C23.550.759]
add_circle
Postoperative Complications [C23.550.767]
add_circle
Protein Aggregation, Pathological [C23.550.770]
Respiratory Aspiration [C23.550.773]
add_circle
Retropneumoperitoneum [C23.550.794]
Sclerosis [C23.550.823]
Shock [C23.550.835]
add_circle
Teratogenesis [C23.550.863]
Toxic Optic Neuropathy [C23.550.877]
Ulcer [C23.550.891]
Vascular Remodeling [C23.550.918]
Yang Deficiency [C23.550.945]
Yin Deficiency [C23.550.972]
All MeSH Categories
Phenomena and Processes
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Mutation [G05.365.590]
Allelic Imbalance [G05.365.590.029]
add_circle
Base Pair Mismatch [G05.365.590.060]
Chromosome Aberrations [G05.365.590.175]
Abnormal Karyotype [G05.365.590.175.024]
add_circle
Aneuploidy [G05.365.590.175.050]
add_circle
Chimerism [G05.365.590.175.125]
Chromosomal Instability [G05.365.590.175.165]
add_circle
Chromosome Breakage [G05.365.590.175.175]
Chromosome Duplication [G05.365.590.175.183]
add_circle
Chromosome Inversion [G05.365.590.175.190]
Chromothripsis [G05.365.590.175.310]
Isochromosomes [G05.365.590.175.430]
Micronuclei, Chromosome-Defective [G05.365.590.175.570]
Mosaicism [G05.365.590.175.595]
Polyploidy [G05.365.590.175.677]
add_circle
Ring Chromosomes [G05.365.590.175.760]
Sex Chromosome Aberrations [G05.365.590.175.815]
add_circle
Translocation, Genetic [G05.365.590.175.870]
add_circle
Uniparental Disomy [G05.365.590.175.935]
Codon, Nonsense [G05.365.590.195]
DNA Repeat Expansion [G05.365.590.220]
add_circle
Frameshift Mutation [G05.365.590.265]
Gain of Function Mutation [G05.365.590.288]
Gene Amplification [G05.365.590.310]
Gene Duplication [G05.365.590.320]
Genomic Instability [G05.365.590.335]
add_circle
Germ-Line Mutation [G05.365.590.350]
INDEL Mutation [G05.365.590.500]
Loss of Function Mutation [G05.365.590.538]
Mutagenesis, Insertional [G05.365.590.575]
Mutation Accumulation [G05.365.590.594]
Mutation Rate [G05.365.590.612]
Mutation, Missense [G05.365.590.650]
Point Mutation [G05.365.590.675]
Sequence Deletion [G05.365.590.762]
add_circle
Sequence Inversion [G05.365.590.770]
add_circle
Silent Mutation [G05.365.590.803]
Suppression, Genetic [G05.365.590.835]
Synthetic Lethal Mutations [G05.365.590.917]
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)