Human Genetics

E890469

Human Genetics is the scientific field that studies how genes and heredity influence human traits, health, and disease.

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Human Genetics canonical 1

Statements (58)

Predicate Object
instanceOf scientific discipline
subfield of biology
subfield of genetics
aimsTo identify genetic risk factors for disease
improve prevention and treatment of human diseases
understand how genes influence human health
appliedIn development of targeted therapies
diagnosis of genetic diseases
forensic genetics
personalized medicine
prevention of genetic disorders
public health genetics
concerns ethical issues in genetic testing
genetic discrimination
privacy of genetic information
focusesOn DNA structure and function in humans
cancer genetics in humans
carrier screening in humans
chromosomal disorders in humans
chromosomes in humans
clinical genetics
complex diseases in humans
genetic counseling
genetic epidemiology of human disease
genetic risk assessment in humans
human evolutionary genetics
human genome organization NERFINISHED
medical genetics
monogenic disorders in humans
multifactorial inheritance in humans
newborn genetic screening
non-Mendelian inheritance in humans
patterns of Mendelian inheritance in humans
pharmacogenetics in humans
pharmacogenomics in humans
polygenic traits in humans
population genetics of humans
prenatal genetic diagnosis
relatedTo bioethics
biostatistics
epigenetics
genomics
molecular biology
studies genetic basis of human disease
genetic variation in humans
gene–environment interactions in humans
human genes
human heredity
inheritance of human traits
usesMethod DNA sequencing
bioinformatics analysis of human genomes
cytogenetic analysis
exome sequencing
family pedigree analysis
genome-wide association studies
linkage analysis
molecular diagnostics
whole-genome sequencing

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