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Genomics & Proteomics

Natural Standard does not recommend specific therapies or practitioners.
This database is purely informational. Website last updated 3/19/2010.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

A
13+ syndrome
2D PAGE
5-fluorouracil
5-FU
5p minus syndrome
5p- syndrome
6-mercaptopurine
Absent radius
ACE genotyping
Achondroplasia
Achondroplastic dwarfism
Achromatopsia
Acid maltase deficiency
Acquired achromatopsia
Acquired hemophilia
Acquired TMAU
Acrocephalosyndactyly type 1 (ACS1)
Active genes
Acute chest crisis
ADA deficiency
Adenine
Adenomatous polyposis coli
Adenosine deaminase deficiency
ADH-resistant diabetes insipidus
Adiposis dolorosa
ADPKD
Adult onset spinal muscular atrophy
Adult TSD
Adult-onset Krabbe disease
Agarose gel electrophoresis
Agitation in dementia
Aicardi syndrome
AKU
Albinism
Alcoholism and genetics
Alkaptonuria
Alleles
Alobar holoprosencephaly
Alpha thalassemia major
Alpha thalassemia minor
Alpha-1 antitrypsin deficiency
Alpha-1 related emphysema
Alpha-L-iduronidase deficiency
Alpha-thalassemia
ALPS
Alzheimer's dementia
Alzheimer's disease (AD)
Amino acids
Amplichip®
Anders’ syndrome
Androgen insensitivity syndrome
Androgen resistance syndrome
Aneuploidy
Angiofibromas
Angiomyolipomas
Angiotensin converting enzyme (ACE) genotyping
Anhidrosis
Antagonistic epistasis
Antibody detecting
Anticancer oligonucleotides
Antiphospholipid syndrome
Antisense oligonucleotide therapy
Antiviral oligonucleotides
APC gene mutation
Apert syndrome
APLA
Aplastic crisis
APLS
APS
Arginase (ARG) deficiency
Argininosuccinase acid lyase (ALD) deficiency
Argininosuccinic acid synthetase (ASD) deficiency
Arrhythmogenic right ventricular cardiomyopathy
Arrhythmogenic right ventricular dysplasia
ARVC
ARVD
Arylamine N-acetyltransferase gene polymorphism
Aspartoacylase deficiency
Asperger syndrome
Asperger’s syndrome
A-T
Ataxia telangiectasia
Autoimmune lymphoproliferative syndrome
Automated nucleic acid extraction
Automated ribotyping
Autosomal dominant disease
Autosomal dominant PKD
Autosomal dominant polycystic kidney disease
Autosomal recessive disorders
Azathioprine
[Top]

B
B variant GM2 gangliosidosis
Barth syndrome
Bartholin-Patau syndrome
Baughman syndrome
BChE
Bean syndrome
Becker muscular dystrophy
Begnez-Cesar's syndrome
Behavioral genetics
Benign tumors
Berlin breakage syndrome
Beta thalassemia
Beta thalassemia intermedia
Beta thalassemia minor
Beta-thalassemia
Beuren syndrome
Biolistic particle delivery
Biolistics
Biological markers
Biological tumor markers
Biomarkers
Biosensors
Biovular twins
Bisulfite sequencing
Black urine
Blue rubber bleb nevus syndrome
BMD
Bourneville’s disease
Bowed legs
Bowel infarction
Brain bleeding
BRBNS
Breast aplasia
Breast cancer
Breast hypoplasia
Brittle bone disease
Brownian motion
Brugia malayi
Brugia timori
Butyrylcholinesterase gene polymorphism
[Top]

C
CAIS
Canavan disease (CD)
Canavan’s leukodystrophy
Canavan-Van Bogaert-Bertrand disease
Cancer chemotherapy
Capillary electrochromatography
Capillary electrophoresis
Capillary electrophoresis
Carbamoyl phosphate synthetase (CPS) deficiency
Cardiac rhabdomyomas
Carriers
Cat cry syndrome
Catastrophic antiphospholipid syndrome
CD
CEC
Cell biology
Cell membrane
Cellular division
CF
CFND
CFNS
Cftr knockout mouse
CHANDS
Charcot-Marie-Tooth disease
Chediak-Higashi syndrome (CHS)
Chemotherapy
Chiari II malformation
Chiral separation
Christmas disease
Chromatin immunoprecipitation
Chromogenic in situ hybridization
Chromosomal abnormalities
Chromosome 16 deletion
Chromosome 5p deletion syndrome
Chromosome banding
Chromosome microdissection
Chromosomes
Chronic SMA
CHS
Cilia
CIPA
Circulating nucleic acids
CISH
Citrin deficiency (citrullinemia II)
Claw hand
Clinical proteomics
Cloning
CMT
Cole-Rauschkolb-Toomey syndrome
Colon cancer
Color blindness
Colorectal cancer
Combined immunodeficiency
Comparative genomics
Complete androgen insensitivity syndrome
Conformation-sensitive gel electrophoresis
Congenital achromatopsia
Congenital hearing loss
Congenital ichthyosis
Congenital insensitivity to pain with anhidrosis
Conjoined twins
Constitutional hepatic dysfunction
Conventional two-color cross-correlation FCS
Cooley’s anemia
Craniofrontonasal syndrome
Craniosynostosis
CREBBP gene mutation
Cri du chat syndrome
Cross-bred pea plants
Cross-correlation spectroscopy
CSGE
Curly hair-ankyloblepharon-nail dysplasia
Cutaneous syndactyly
Cylium
CYP1A2 gene
CYP1A2*1F gene
CYP2D6 and CYP1A2*1F Genotyping
CYP2D6 gene
CYP450 gene
Cystic eyelids-palmoplantar keratosis-hypodontia-hypotrichosis
Cystic fibrosis (CF)
Cystic fibrosis knockout mouse model
Cystinosis
Cytogenetics
Cytogenic maps
Cytoplasm
Cytosine
[Top]

D
Dark urine
DBMD
Dejerine-Sottas syndrome
Dento-oculo-osseous dysplasia
Deoxyribonucleic acid
Dercum’s disease
Dermatofibromas
Dermatopathia pigmentosa reticularis
Dermoodontodysplasia
Dermotrichic syndrome
Desmoid colon tumor
Diabetes
Diabetes insipidus renalis
Diabetes mellitus type 1
Diabetes mellitus type 2
Diabetic complications
Diabetic foot pain
Diabetic ketoacidosis
Diabetic microangiopathy
Diabetic nephropathy
Diabetic neuropathy
Diabetic peripheral neuropathy
Diandry
Dichorionic diamniotic twins
DIDMOAD syndrome
Digyny
Digyny triploidy
Disease onset biomarkers
Disease proteomics
Disproportionate dwarfism
Dizygotic twins
DKC
DMD
DNA
DNA expression
DNA markers
DNA microarray technology
DNA patenting
DNA sequencing and sequence variation
Dominant allele
Double helix
Down syndrome
DR syndrome
Drug addiction and genetics
Drugs and genetics
Duane syndrome
Duchenne muscular dystrophy
Dyskeratosis congenita
DZ twins
[Top]

E
E3 trisomy
Ectodermal dysplasia-exocrine pancreatic insufficiency
Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome
Edwards syndrome
EEC syndrome
EEC syndrome 1
EEC syndrome 2
EEC syndrome 3
Electrophoresis
Electrophoretic mobility shift assay
Elephantiasis
Elephantitis
Elfin facies syndrome
Ellis-Van Creveld Syndrome
Endocardial cushion defect
Environmental Genome Project
EP300 gene mutation
Epigenetic modification
Epigenetics
Epistasis
Epistatic
EST patenting
Ethical issues in genetic research
Eugenics
Eukaryote
EVC syndrome
Excessive bleeding
ExInt™
Exon
Exon-Intron™ database
Exostoses
Expressed sequence tag patenting
Expressed sequence tags
Extragonadal germ cell tumors
Eye cancer
[Top]

F
Facioscapulohumeral muscular dystrophy
Factor IX deficiency
Factor IX hemophilia
Factor VIII deficiency
Factor X deficiency
Factor XI deficiency
Familial adenomatous polyposis
Familial dysautonomia type II
Familial holoprosencephaly
Familial Mediterranean Fever (FMF)
Familial nonhemolytic jaundice
Family History Initiative
FAP
FCS
Fibrodysplasia ossificans progressiva (FOP)
FISH
Fish odor syndrome
Flagella
Fluorescence correlation spectroscopy
Fluorescence in situ hybridization (FISH)
FMF
Folling's disease
FOP
Fragile X syndrome (FXS)
Francis Crick
Fraternal twins
Frontonasal dysplasia syndrome
FSHD
Functional genomics
FX deficiency
FXI deficiency
FXS
[Top]

G
G6PD deficiency
Galactose-1-phosphate uridyl transferase deficiency
Galactosemia
Gargoylism
Gastrointestinal tract and colorectal cancer prevention
Gaucher disease
G-banding
GCL
Gel electrophoresis
Gene expression analysis
Gene gun technology
Gene therapy
GeneChip®
Gene-nutrient interactions
Genes linked to drug addiction
Genetic biomarkers
Genetic biosensors
Genetic carriers
Genetic discrimination
Genetic disease prevention and treatment
Genetic disorders
Genetic diversity
Genetic Information Nondiscrimination Act
Genetic Nondiscrimination Act
Genetically engineered foods
Genetically modified foods (GMFs)
Genetically modified organisms (GMOs)
Genetics and patenting
Genetics and the nervous system
Genetics overview
Genomic biomarkers
Genomic sequencing
Genomics in clinical practice
Genomics overview
Genotype
Genotyping
Genu varum
Gestational diabetes
Gibbus deformity
Giemsa staining
Gilbert’s syndrome
Globoid cell leukodystrophy
Glucocerebrosidase deficiency
Glucose 6-phosphate dehydrogenase deficiency
Glucose intolerance
Glycogen storage disease
Glycogen storage disease type II
GM2 gangliosidosis adult chronic type
GM2 gangliosidosis type 1
GMFs
GMOs
Golgi apparatus
Golgi complex
Gowers’ sign
Gregor Mendel
Guanine
[Top]

H
H19 gene
Hand-held gene gun
HbS disease
HbSC disease
HbSE disease
Helios™ gene gun
Hemangioma
Hematochezia
Hematuria
Hemoglobin H disease
Hemoglobin S disease
Hemophilia
Hemophilia A
Hemophilia B
Hemophilia C
Heparan sulfate sulfatase deficiency
Hereditary colon polyposis
Hereditary motor sensory neuropathy
Hereditary multiple exostoses type 1
Hereditary sensory and autonomic neuropathy type IV
Heredity
Heterosis
Heterotopic ossification
Heterozygous
Hexosaminidase A deficiency
HGP
HGPS
HHH syndrome
HIES
High blood sugar levels
High-functioning autism
High-performance liquid chromatography
High-throughput tissue analysis
HND
Holoprosencephaly (HPE)
Holoprosencephaly malformation complex
Hoveraal-Hreidarsson syndrome
HPE
Hughes syndrome
Human Genome Project (HGP)
Huntington's chorea
Huntington's disease
Hurler syndrome
Hurler-Scheie syndrome
Hutchinson-Gilford progeria syndrome (HGPS)
Hybrid vigor
Hybridization
Hydrocephalus
Hydrops fetalis
Hyperalaninemia
Hyperammonemia
Hyperglycemia
Hyperimmunoglobulin E syndrome
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)
Hypodontia
Hypodontia and nail dysgenesis
Hypohidrosis
Hypostatic
Hypotrichosis
[Top]

I
IBC
Identical twins
IgE syndrome
IGF2 gene
Immunohistochemistry
Imprinting
In situ hybridization (ISH)
Inborn errors of urea synthesis
Inbreeding depression
Infantile FSHD
Infantile hypercalcemia
Infantile TSD
Infantile-onset SMA
Inflammatory breast cancer (IBC)
Inherited bleeding disorder
Inherited disease prevention and treatment
Inherited disorders
Inherited emphysema
Insulin Resistance Syndrome (IRS)
Interferometer
Intergenic regions
Intron
Intussusception
Irinotecan
IRS
ISH
Isolated holoprosencephaly
Isolated patent ductus arteriosus
[Top]

J
James Watson
JBS
Job syndrome
Job-Buckley syndrome
Johanson-Blizzard syndrome
Joint bleeding
Junk DNA
Juvenile Krabbe disease
Juvenile SMA
Juvenile TSD
[Top]

K
Karyology
Karyotype analysis
Kearns-Sayre syndrome
Keratosis palmoplantaris
Klein-Waardenburg syndrome
Klinefelter syndrome
Knockout mice
Krabbe disease
Kugelberg-Welander disease
[Top]

L
Landouzy-Dejerine muscular dystrophy
Langer-Giedion syndrome
Large-Scale Genome Sequencing Program
Late infantile Krabbe disease
Late onset TSD
Leigh’s disease
LGS
Li-Fraumeni syndrome
Ligase chain reaction
Lipomatosis dolorosa
Livedo reticularis
Lobar holoprosencephaly
Lordosis
LOTS
Lumbosacral spinal stenosis
Lymphatic filariasis
Lysosomal storage disease
[Top]

M
Magic roundabout4
MALDI imaging team imaging computing system
MALDI Molecular Imager™
MALDI-TOF mass analyzer
MALDI-TOF mass spectrometry
Manual ribotyping
Maple syrup urine disease (MSUD)
Maroteaux-Lamy syndrome
Martin-Bell syndrome
Matrix-assisted laser desorption/ionization time-of-flight
Maturity-onset diabetes of the young (MODY)
McArdle's disease
Meckel’s diverticulum
Median cleft-face syndrome
Mediterranean anemia
Medullary carcinoma
Meiosis
MELAS syndrome
Mendelian genetics
Mendel's principles
Meningocele spina bifida
Messenger RNA
Metabolic biomarkers
Metabolic disorders
Metabolic syndrome
Metaphyseal chondrodysplasia
Microarray technology
Microwave-assisted enzyme digestion
Midline cleft syndrome
MITICS
Mitochondria
Mitochondrial biogenesis
Mitochondrial DNA
Mitochondrial genome
Mitosis
MODY
Molecular biology
Molecular genetics in clinical practice
Mongolian spots
Monitoring biomarkers
Monochorionic diamniotic twins
Monochorionic monoamniotic twins
Monogenic disorders
Monozygotic twins
Morgagni-Turner-Albright syndrome
Morquio syndrome
Mosaic Down syndrome
Mosaic Klinefelter syndrome
Mosaic trisomy 18
Mosaic Turner syndrome
Mouse genome
MPS
MPS H-S
MPS I H
MPS I S
MPS type 3
mRNA
MSUD
mtDNA
mtDNA somatic mutations
mtgenome
Mucinous carcinoma
Mucopolysaccharidosis
Mucopolysaccharidosis III
Mucoviscidosis
Muenke nonsyndromic coronal craniosynostosis
Muenke syndrome
Multicolor-FISH
Multiple births
Multiple pregnancy
My Family Health Portrait
Myelodysplastic syndrome (MDS)
Myelomeningocele spina bifida
MZ twins
[Top]

N
N-acetylglutamate synthetase (NAGS) deficiency
Naegeli-Franceschetti-Jadassohn syndrome
Nail dysplasia
NAT1 gene
NAT2 gene
Nature versus nurture controversy
Naxos disease
NBS
NDI
Nephrogenic diabetes insipidus
Neural tube defects
Neurogenetics
Neurolipomatosis
Neuronal patterning
NFJ syndrome
Nijmegen breakage syndrome
Nitrogenous bases
Noncancerous tumors
Noncoding DNA
Nondisjunction
Non-identical twins
NTDs
Nucleic acid extraction
Nucleic acid sequenced-based amplification
Nucleic acids
Nucleus
Nutrigenetics
Nutrigenomics
Nutritional genomics
[Top]

O
Occurrence biomarkers
Ochronosis
Oculocutaneous albinism
Oculodentodigital syndrome
ODD
ODOD
OFD I
OI
Oligonucleotide antiviral medications
Oligonucleotide design for PCR primers and microarray probes
Oligonucleotide microarrays in microbial diagnostics
Oligonucleotide therapy
Oligonucleotide-based medicine
Oligonucleotides
Onchorosis
Oncosuppressor gene
Organelle
Ornithine transcarbamylase (OTC) deficiency
Ornithine translocase deficiency
Orofaciodigital syndrome type I
Ossification
Osteogenesis imperfecta
Outbreeding depression
Outbreeding enhancement
Ovarian dwarfism
Ovarian hypofunction
Overview of genetic disorders
[Top]

P
P53 gene
PAGE
PAIS
Palmoplantar keratoderma
Papillon-Leage-Psaume syndrome
Parkinson's disease
Partial androgen insensitivity syndrome
Particle bombardment
Particle-mediated gene transfer
Patau syndrome
Peroneal muscular atrophy
Personalized medicine
Pharmacogenetics
Pharmacogenomics
Phenotype
Phenylketonuria (PKU)
Phospholipid antibody syndrome
PKU
Plantar hyperplasia
Plasma membrane
Plasma thromboplastin antecedent deficiency
Plate reader
Poland anomaly
Polyacrylamide gel electrophoresis
Polymorphisms of the BChE gene
Polyploidy
Pompe disease
Population proteomics
Precursor overload TMAU
Premature aging syndrome
Primary genetic TMAU
Principle of independent assortment
Principle of segregation
Progeria
Prokaryote
Prostate cancer
Protein biomarkers
Protein expression profiling
Proteome
Proteomic biomarkers
Proteomics
Proteus syndrome
Protoplast transformation
Pseudocholinesterase deficiency
Pseudohypertrophic muscular dystrophy
Pseudomonas infection in cystic fibrosis
Pulse-field gel electrophoresis
Pyruvate carboxylase deficiency
[Top]

Q
[Top]

R
Radial aplasia-thrombocytopenia syndrome
Radial club hand
RCA
Recessive allele
Recessive disorders
Recombinant DNA technology
Recurrent polyserositis
Reifenstein syndrome
Reproductive cloning
Resistance to tetracycline
Retinoblastoma
Retraction syndrome
Rett syndrome
Rib cage abnormalities
RiboBank
Riboprinter® system
Ribosome protection
Ribosomes
Ribotyping
RNA
RNA interference (RNAi)
RNAi
Robo genes
Robo1 gene
Robo2 gene
Robo3 gene
Robo4 gene
Rolling-circle amplification (RCA)
Rosenthal's syndrome
Roundabout4 gene
RSTS
Rubinstein syndrome
Rubinstein-Taybi syndrome (RSTS)
[Top]

S
Safety biomarkers
SAGE
Sanfilippo syndrome
Scheie syndrome
Schereshevkii-Turner syndrome
Schopf-Schulz-Passarge syndrome
SCID
SDA
SDS
SDS-PAGE
SDS-polyacrylamide gel electrophoresis
Semilobar holoprosencephaly
Sequencing DNA
Serial analysis of gene expression
Severe combined immunodeficiency
Short-limbed dwarfism
Shwachman syndrome
Shwachman-Bodian syndrome
Shwachman-Diamond syndrome
Sickle beta-plus-thalassemia
Sickle beta-zero-thalassaemia
Sickle cell anemia
Sickle cell disease
Sickle-hemoglobin C disease
Sickle-hemoglobin E disease
Single gene disorders
Single nucleotide polymorphism
Single-phase single-molecule fluorescence correlation spectroscopy
Skin cancer
SKY
Sly syndrome
SMN1 gene mutation
SN-38
SNP
Soft ionization
Solution-phase single-molecule fluorescence
Somatic cell nuclear transfer
Species-specific behavior
Spectral karyotyping
Spina bifida
Spina bifida manifesta
Spina bifida occulta
Spinal muscular atrophy
Spinal stenosis
SPSM-FCS
Staging biomarkers
Strand displacement amplification
Stuart-Prower deficiency
Subacute necrotizing encephalopathy
Surrogate markers
Syndrome X
Synergistic epistasis
[Top]

T
TAR syndrome
Target biomarkers
Targeted therapies
Tay-Sachs disease
Tay-Sachs disease (TSD)
Telomerase
Telomere therapy
Telomeres
TetA gene
TetB gene
TetC gene
Tethered spinal cord
TetM gene
Tetracycline efflux
Tetracycline modification
Tetracycline resistance
Tetralogy of fallot
Tetraphocomelia-thrombocytopenia syndrome
Tetraploidy
Thalassemia
Thalassemia intermedia
Thalassemia major
Thalassemia minor
Therapeutic cloning
Therapeutic genes
Thioguanine
Thiopurines
Thrombocytopenia absent radius syndrome
Thymine
Time-of-flight (TOF) analyzers
Tissue microarrays
TMAU
TMAuria
Tourette’s syndrome
Toxicity biomarkers
Toxicogenomics
Transcription-mediated amplification
Transcriptome
Transcriptomics
Transfection
Transient childhood TMAU
Transient menstrual TMAU
Translocation Down syndrome
Trichinellosis
Trichinosis
Tricho-rhino-phalangeal syndrome type 1
Trichorhinophalangeal syndrome type II
Trimethylaminuria
Triploidy
Trisomy 13
Trisomy 18
Trisomy 21
TRPS2
TSC
TSD
Tuberous sclerosis
Tuberous sclerosis complex
Tubular carcinoma
Tumor suppressor gene
Turner syndrome
Turner-Varny syndrome
Twin studies
Twinning
Twins
Two-dimensional electrophoresis
Type 1 diabetes
Type 2 diabetes
Type I SMA
Type II SMA
Type III SMA
Type IV SMA
[Top]

U
Ullrich-Turner syndrome
Ultraviolet skin damage protection
Unconjugated benign bilirubinemia
Unilateral radial aplasia
Urea cycle disorders
[Top]

V
Valgus deviation
Van Bogaert-Bertrand syndrome
Vaso-occlusive crisis
Vasopressin-resistant diabetes insipidus
Vesicle
Viral vectors
Vitravene®
[Top]

W
Waardenburg syndrome
Waardenburg-Shah syndrome
WAS
Werdnig-Hoffman disease
Western blotting
White pupils
Wiedemann’s dysmelia syndrome
Wiedemann’s syndrome
Williams syndrome
Williams-Beuren syndrome
Wilson’s disease
Wiskott-Aldrich syndrome
Witkop’s syndrome
WMS
Wolfram syndrome
Wolhlfart-Kugelberg-Welander disease
WS
Wuchereria bancrofti
[Top]

X
X-linked infantile spinal-muscular atrophy
X-linked recessive disorders
XL-SMA
XO syndrome
XXXY syndrome
XXY males
XXY trisomy
[Top]

Y
[Top]

Z
Zinsser-Engman-Cole syndrome
[Top]