- chromosome defect
- ˈchro·mo·some de·fectadj Chromosomenschaden m, Chromosomendefekt m
English-german dictionary. 2013.
chromosome defect
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Chromosome 16 (human) — Chromosome 16 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 16 spans about 90 million base pairs (the building material of DNA) and represents just under 3 % of the total DNA… … Wikipedia
Chromosome 1, 1p36 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34535 ICD10 = ICD9 = ICDO = OMIM = 607872 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = MeshID = Chromosome 1, 1p36 deletion syndrome is a medical condition caused by a rare … Wikipedia
Chromosome 15 (human) — Human chromosome 15 Chromosome 15 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 15 spans about 106 million base pairs (the building material of DNA) and represents between 3% and 3 … Wikipedia
Congenital heart defect — Classification and external resources The normal structure of the heart (left) in comparison to two common locations for a ventricular septal defect (right), the most common form of congenital heart defect.[1] … Wikipedia
Y chromosome — Human Y chromatid The Y chromosome is one of the two sex determining chromosomes in most mammals, including humans. In mammals, it contains the gene SRY, which triggers testis development if present. The human Y chromosome is composed of about 60 … Wikipedia
Y chromosome microdeletion — (YCM) is a family of genetic disorders caused by missing gene(s) in the Y chromosome. Many men with YCM exhibit no symptoms and lead normal lives. However, YCM is also known to be present in a significant number of men with reduced fertility. Men … Wikipedia
Philadelphia chromosome — Infobox Disease Name = Philadelphia chromosome Caption = A metaphase cell positive for the bcr/abl rearrangement using FISH DiseasesDB = ICD10 = ICD10|C|92|1|c|81 ICD9 = ICD9|205.1 ICDO = 9875/3 OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic … Wikipedia
Syndrome, chromosome 4 short-arm deletion — This syndrome, called the Wolf Hirschhorn syndrome, is a chromosome disorder due to partial deletion of the short (p) arm of chromosome 4. It is, therefore, also called the 4p syndrome. Features of the syndrome include midline defects with a… … Medical dictionary
Thyroid hormone organification defect IIb — This condition, clinically called Pendred syndrome, is the hereditary association of congenital deafness (deafness at the time of birth) and goiter (enlargement of the thyroid gland in the front of the neck) due to a defect in the making of… … Medical dictionary
blood disease — Introduction any disease of the blood, involving the red blood cells (erythrocytes (erythrocyte)), white blood cells (leukocytes (leukocyte)), or platelets (platelet) (thrombocytes) or the tissues in which these elements are formed the bone … Universalium
XYY syndrome — Not to be confused with XXY (2 X s, Klinefelter s syndrome). XYY syndrome Classification and external resources Y chromosome ICD 10 Q … Wikipedia
