Category:Genetics
From WikiMD.com Medical Encyclopedia
(Redirected from Category:Genetic diseases)
Genetics is the study of genes, heredity, and the variation of organisms, as well as the medical practice of diagnosing, treating, and counseling patients with genetic disorders. Humans began applying knowledge of genetics in prehistory with the domestication and breeding of plants and animals. In modern research, genetics provides important tools in the investigation of the function of a particular gene, e.g. analysis of genetic interactions. Within organisms, genetic information generally is carried in chromosomes, where it is represented in the chemical structure of particular DNA molecules.
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Subcategories
This category has the following 21 subcategories, out of 21 total.
A
C
D
E
G
H
J
M
N
O
P
Σ
Pages in category "Genetics"
The following 200 pages are in this category, out of 1,568 total.
(previous page) (next page)A
- ABC model of flower development
- Aberrations
- Abnormality
- Acentric fragment
- Achaete-scute complex
- ACT
- Activator
- Activator (genetics)
- Active chromatin sequence
- Activin receptor
- ADAMTS
- Additive genetic effects
- Adenomatous polyposis coli
- AFLP
- Agouti-signaling protein
- AGXT
- Aicardi–Goutières syndrome
- ALDH2
- ALG3
- ALIL pseudoknot
- Allele
- Allele frequency
- Allelic exclusion
- Allelic heterogeneity
- Allotype (immunology)
- Alpha-actinin-3
- Alteration
- Alterations
- Alternative splicing
- Alu
- Alu element
- ALX4
- AMELX
- AMELY
- Amidophosphoribosyltransferase
- Amplicon
- Amplification
- Amsterdam criteria
- Anaphase
- Anaphase lag
- Androgenesis
- Aneugen
- Aneuploidy
- Animal breeding
- ANKH
- Antagomir
- Antagonistic pleiotropy hypothesis
- Antennapedia
- Anti-CRISPR
- Anticancer gene
- Anticipation
- Anticipation (genetics)
- Antimutagen
- Antisense RNA
- Antitermination
- Stylianos Antonarakis
- APC
- Apomixis
- Apoprotein
- Archaeogenetics
- Arrhenotoky
- Artificial gene synthesis
- Assortative mating
- Atavism
- ATBF1
- ATRX
- Attenuated
- Autism Genetic Resource Exchange
- Autism Research
- Autism Research Centre
- Autogamy
- Autosome
- Auxology
- Auxotrophy
- AX
B
- B chromosome
- Bacillus subtilis
- Back mutation
- Backcrossing
- Bacterial conjugation
- Bacterial genetics
- Bacterial transcription
- Balancing selection
- Baldwin effect
- Barr body
- Base pair
- BBS5
- BC200 lncRNA
- BCKDHA
- BCKDHB
- Behavioral epigenetics
- Behavioural genetics
- Bernhard Landwehrmeyer
- Bicoid 3′-UTR regulatory element
- BIN1
- Binucleated cells
- Biobank
- BioImpacts
- Biological determinism
- Biological inequity
- Biological material
- Biological pathway
- Biology of Sex Differences
- Biorientation
- Biotype
- Biparental inheritance
- Blaschko's lines
- Blending inheritance
- Blood line
- Blood purity
- Blunt end
- Boveri–Sutton chromosome theory
- Brachy
- BRCA mutation
- Breakage-fusion-bridge cycle
- Breed
- Breeder
- Breeding
- Breeding program
- BRN-3
- Bruton's tyrosine kinase
- Buccal swab
C
- C1330-7
- C9orf72
- CACNA2D2
- Caenorhabditis
- Caenorhabditis elegans
- Caenorhabditis elegans Cer1 virus
- Calico cat
- Cambridge University primates
- Canalisation (genetics)
- Candidate gene
- Carbamoyl phosphate synthetase I
- Carbonic anhydrase
- Carnitine O-acetyltransferase
- Carnitine palmitoyltransferase II
- Carrier
- Cas9
- Cat genetics
- Catechol-O-methyltransferase
- Cav1.2
- Cav2.1
- CDNA library
- Cdx
- Cell Cycle
- Cell cycle checkpoint
- Cell-free fetal DNA
- CENPA
- Central dogma of molecular biology
- Centromere
- Chargaff's rules
- Charles Usher
- Chi site
- Chiasma
- Chicken as biological research model
- Children's Medical Research Institute
- Chimera
- Chimera (genetics)
- Chimeric RNA
- CHL1
- Chloroplast DNA
- CHMP2B
- CHRNA2
- CHRNB1
- CHRND
- Chromatid
- Chromatin
- Chromatin immunoprecipitation
- Chromatin remodeling
- Chromatosome
- Chromomere
- Chromosomal crossover
- Chromosomal fragile site
- Chromosomal inversion
- Chromosomal rearrangement
- Chromosomal translocation
- Chromosome 1, uniparental disomy 1q12 q21
- Chromosome 10
- Chromosome 11-14 translocation
- Chromosome 12
- Chromosome 13
- Chromosome 14
- Chromosome 15
- Chromosome 18
- Chromosome 19
- Chromosome 2
- Chromosome 20
- Chromosome 21
- Chromosome 22
- Chromosome 2q deletion
- Chromosome 4
- Chromosome 5
- Chromosome 8
- Chromosome instability
- Chromosome segregation
- Chromothripsis
- Circular chromosome
- Circulating mitochondrial DNA
- Cis AB
- Cis-regulatory element
