Personalised medicine

Personalised medicine is choosing treatment or disease prevention strategy, specifically for the individual patient. The term has evolved to mean the use of molecular genetic information to tailor such therapy. This includes the identification of molecular features of host, parasite or cancer cell, which help to predict the patient's risk-category and likely response to therapy, either beneficially or adversely.

Teaching Genetics

• Teaching Home
• Medical Practitioners
• Nursing Professions
• Pharmacogenetics
• Dietitians
• Glossary

  • Alleles

  • Amniocentesis

  • Anticipation

  • Autosomal dominant

  • Autosomal recessive

  • Autosome

  • Carrier

  • Carrier screening

  • Carrier testing

  • Chorionic Villus Sampling

  • Chromosome

  • Clinical genetics

  • Clinical Utility

  • Clinical Validity

  • Clone

  • Coding sequence

  • Codon

  • Companion diagnostic

  • Congenital

  • Consanguineous

  • Copy Number Variation (CNV)

  • Cytogenetics

  • De novo mutation

  • Degree of relationship

  • Direct mutation detection

  • DNA

  • DNA linkage studies

  • DNA testing

  • Dysmorphic

  • Empiric risk

  • Epigenetic

  • Expressivity

  • Family Tree

  • First-degree relative

  • FISH: fluorescence in situ hybridisation

  • Gamete

  • Gene

  • Gene deletion(s)

  • Gene inversion

  • Gene signature

  • Gene tracking

  • Genetic

  • Genetic counselling

  • Genetic heterogeneity

  • Genetic Predisposition

  • Genetic Susceptibility

  • Genetics

  • Genome

  • Genome-wide Association Study (GWAS)

  • Genomic medicine

  • Genotype

  • Gonadal/germline mosaicism

  • GWAS

  • Heterozygote (Heterozygous): Carrier

  • Homologous

  • Homozygote (Homozygous)

  • Incidence

  • Inheritance

  • Karyotype

  • Liability

  • Linkage analysis

  • Locus (loci)

  • Malformation

  • Marker

  • Mendelian inheritance

  • Mitochondria

  • Mitochondrial condition

  • Mitochondrial inheritance

  • Monosomy (Monosomic)

  • Mosaicism (mosaic)

  • Multifactorial inheritance

  • Mutation

  • New mutation

  • Offspring risk

  • Patterns of inheritance

  • Pedigree diagram

  • Penetrance

  • Personalised medicine

  • Pharmacogenetics

  • Pharmacogenomics

  • Phenotype

  • Polymerase chain reaction (PCR)

  • Polymorphism

  • Premutation

  • Prenatal diagnosis

  • Presymptomatic testing

  • Prevalence

  • Recurrence risk

  • Second-degree relative

  • Sex chromosome

  • Sib/sibling

  • Single gene disorder

  • Somatic cell

  • Sporadic

  • Stratified medicine

  • Syndrome

  • Teratogen

  • Third-degree relative

  • Trait

  • Transcription

  • Translation

  • Translocation

  • Trinucleotide (triplet) repeat

  • Trisomy (Trisomic)

  • X-Chromosome inactivation

  • X-linked dominant

  • X-linked recessive