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Human genome

The human genome consists of 23 chromosome and the small mitochondrial DNA. 22 of the 23 chromosomes are autosomal chromosome pairs and the last one being a gender-determining pair. In total, the human genome contains the sequences of the 3 billion chemical base pairs that make up human DNA and approximately 20,000-25,000 genes. By understanding human genome, scientists are able to develop new medical applications that can significantly advance the state of health care.

Contributors in Human genome

Human genome

graft-versus-host disease

Medical; Human genome

1) A reaction of donated stem cells against the patient's tissue. 2) A bodily condition that results when T cells from a usually allogeneic tissue or organ transplant and especially a bone marrow ...

hermaphrodite

Medical; Human genome

1) An organism having both male and female sexual characteristics and organs. 2) An abnormal individual especially among the higher vertebrates having both male and female reproductive organs -- ...

haplotype map (HapMap)

Medical; Human genome

The nickname of the International HapMap Project, an international project that seeks to relate variations in human DNA sequences with genes associated with health. A haplotype is a set of DNA ...

homologous chromosomes

Medical; Human genome

The two chromosomes from a particular pair, normally one inherited from the mother and one from the father, containing the same genetic loci in the same order.

hyperostosis

Medical; Human genome

Increase in the mass of bone per unit volume.

hepatosplenomegaly

Medical; Human genome

Coincident enlargement of the liver and spleen.

hydrocephalus

Medical; Human genome

1) Excessive accumulation of cerebrospinal fluid within the cranium which may be a congenital or acquired disorder; hydrocephalus ex-vacuo refers to ventricular dilation that occurs as a result of ...

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