Category:Medical genetics

C

• Cancer genomics‎ (2 C, 5 P)

E

• Genetic epidemiology‎ (1 C, 24 P)

G

• Genetic diseases and disorders‎ (14 C, 187 P)

M

• Medical geneticists‎ (1 C, 39 P)
• Medical genetics journals‎ (24 P)
• Microarrays‎ (54 P)

P

• Pathogen genomics‎ (25 P)
• Progeroid syndromes‎ (1 C, 14 P)
• Public health genomics‎ (4 P)

R

• Race and health‎ (2 C, 14 P)

• Medical genetics

*

• Whole genome sequencing

0–9

• 1q21.1 copy number variations
• 100,000 Genomes Project
• 100K Pathogen Genome Project

A

• Amaurosis congenita, cone-rod type, with congenital hypertrichosis
• Amish lethal microcephaly

B

• Biodistribution
• Blepharophimosis intellectual disability syndromes

C

• Cancer Genome Anatomy Project
• Centre for Genomic Pathogen Surveillance
• Consanguine marriage
• Consanguinity
• COSMIC cancer database
• Cryptic relatedness

D

• DECIPHER
• DNA-directed RNA interference
• Double minute
• Duplex sequencing
• Dysmorphic feature

E

• Ensembl genome database project
• Ensembl Genomes
• Exact Sciences Corp.

F

• Functional cloning

G

• GENCODE
• Gene therapy
• Gene therapy for osteoarthritis
• Gene therapy of the human retina
• Genetic counseling
• Genetic diagnosis of intersex
• Genetic Information Nondiscrimination Act
• Genetic screen
• Genetic testing
• Genome-wide complex trait analysis
• Genomic Health
• Grail (company)
• GRaPH-Int

H

• Heritability of autism
• Heritability of IQ
• Human disease modifier gene
• Human HGF plasmid DNA therapy

I

• Immunogenetics
• Inborn errors of immunity
• Inborn errors of metabolism
• Individualized cancer immunotherapy

L

• List of gene therapies

M

• MAGESTIC
• Medical genetic ethics
• Medical genetics of Jews
• Metabolic disorder
• Molecular diagnostics
• Multiple congenital anomalies-hypotonia-seizures syndrome
• Mutalyzer
• Mutanome
• Myriad Genetics

N

• Neoepitope
• Nutritional epigenetics
• Nutritional genomics

O

• Oncogenomics
• List of databases for oncogenomic research

P

• Paternal age effect
• Penetrance
• Point-of-care genetic testing
• Polar body biopsy
• PomBase
• Population structure (genetics)
• Preimplantation genetic diagnosis
• Preimplantation genetic haplotyping
• Prevention of autosomal recessive disorders
• Pseudodeficiency alleles
• Psychiatric genetics

R

• Repoxygen
• The Resilience Project

S

• Savior sibling
• SRD5A3-CDG
• Strimvelis
• Substrate reduction therapy
• Swedish mutation

T

• Therapeutic gene modulation
• Toxicogenomics

V

• Vectors in gene therapy
• Vertebrate Genome Annotation Project

X

• X-linked cone-rod dystrophy, type 1