Monosomy [monozomie]

topical

Persistent link https://www.medvik.cz/link/D009006

Definition

The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1.

DUI: D009006 MeSH Browser
CUI: M0014044
Previous indexing: Chromosome Aberrations (1968-1984); Chromosome Abnormalities (1966-1984); Aneuploidy (1968-1984); Chromosome Deletion (1975-1984)
History note: 91(85); was see under CHROMOSOME DELETION 1985-90
Public note: 91; was see under CHROMOSOME DELETION 1985-90

Allowable subheadings

... Occurrences in Medvik records

C Diseases

C23 Pathological Conditions, Signs and Symptoms 451

C23.550 Pathologic Processes 195

C23.550.210 Chromosome Aberrations 1 574

C23.550.210.050 Aneuploidy 197

C23.550.210.050.500 Monosomy 23

C23.550.210.050.500.500 Chromosome Deletion 199

C23.550.210.050.625 Tetrasomy 2

C23.550.210.050.750 Trisomy 176

G Phenomena and Processes

G05 Genetic Phenomena 135

G05.365 Genetic Variation 858

G05.365.590 Mutation 4 997

G05.365.590.175 Chromosome Aberrations 1 574

G05.365.590.175.050 Aneuploidy 197

G05.365.590.175.050.500 Monosomy 23

G05.365.590.175.050.500.500 Chromosome Deletion 199

G05.365.590.175.050.625 Tetrasomy 2

G05.365.590.175.050.750 Trisomy 176

G05.700 Ploidies 90

G05.700.131 Aneuploidy 197

G05.700.131.500 Monosomy 23

G05.700.131.500.500 Chromosome Deletion 199

G05.700.131.625 Tetrasomy 2

G05.700.131.750 Trisomy 176

Chromosome 18 mosaic monosomy Disease MeSH Browser

Chromosome 21 monosomy Disease MeSH Browser

Chromosome 8 deletion Disease MeSH Browser