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Monosomy
Monosomy
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Topics Related to Monosomy
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Cytogenetics
(19)
Autosomal
Chromosomal disorder
Chromosomal translocation
Chromosome
Karyotype
Karyotype
Partial monosomy
Trisomy
X chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Uniparental disomy
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Genetic disorders
(28)
Monosomy 1p36
Partial monosomy 13q
Myoclonic Epilepsy with Ragged Red Fibers
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis iv
Multiple lentigines syndrome
Mucopolysa- ccharidosis, type I
Mucolipidoses
Turner syndrome
18p deletion syndrome
4p- syndrome
Karyotype 47,XXX
5p- syndrome
MGA type II
Jacobsen syndrome
49 xxxxx syndrome
47,XYY
Warkany syndrome 2
Albright syndrome
Genetic condition
Trisomy 9
Patau syndrome
Craniofacial dysostosis
Trisomy 16
Microcephaly
Partial monosomy
Trisomy
Chromosomal disorder
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Pediatrics
Mucocutaneous lymph node disease
Craniosynostosis
Trisomy 9
Genetic disorder
Myoclonic Epilepsy with Ragged Red Fibers
Warkany syndrome 2
Trisomy 9
Trisomy 16
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Syndromes
(15)
Munchausens syndrome
3-M Syndrome
Myelodysplastic syndromes
Mucopolysa- ccharidosis iii
Multiple lentigines syndrome
Multiple lentigines syndrome
Mucopolysa- ccharidosis, type I
Turner syndrome
18p deletion syndrome
4p- syndrome
Karyotype 47,XXX
5p- syndrome
47,XYY
Warkany syndrome 2
Patau syndrome
Craniofacial dysostosis
more...
Chromosomes
(54)
Chromosome 11
Chromosome 18
Chromosome 22
Chromosome 3
Chromosome 7
Chromosome 7
Chromosome 8
Pericentric inversion
Ring chromosome
Short arm
Subtelomere
AZF1
Allosome
Autosomal
Centromere
Chromatid
Chromomere
Chromosomal disorder
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 4 (human)
Chromosome 5 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Marker chromosome
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Syntelic
Telomere
X chromosome
Y chromosome
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Genetics
Mosaicism
Medical genetics
Chromosomes
47,XYY
Genetic condition
Cytogenetic
Congenital disorders
Malformations
Trigonocephaly
Cystic hygroma
Camptodactyly
18p deletion syndrome
Microcephaly
Medicine
Diseases and disorders
Monorchism
Dysmorphic
Short stature
Camptodactyly
Diseases and disorders
Monosomy 18p
Monosomy 9p
Webbed neck
Growth retardation
Mucopolysa- ccharidosis iv
Symptoms
(10)
Movement dysfunctional
Motormental retardation
Muscle fasciculation
Muscle function loss
Uncoordinated movement
Uncoordinated movement
Mental retardation
Congenital heart defects
Hypotonia
Low set ears
Short stature
more...
Medical condition
(50)
Monosomy x
Chromosome 10 monosomy 10p
Chromosome 18 monosomy 18p
Chromosome 13 partial monosomy 13q
Chromosome 8 monosomy 8p2
Chromosome 8 monosomy 8p2
Chromosome 3 monosomy 3p2
Chromosome 4 monosomy distal 4q
Chromosome 4 monosomy 4q
Chromosome 9 partial monosomy 9p
Chromosome 7 partial monosomy 7p
Myotonia atrophica
Myxomatous mitral valve
Infectious mononucleosis
18p syndrome
Ovarian dwarfism
Chromosome 9 tetrasomy 9p
Gonadal dysgenesis
Congenital hypomyelination
Chromosome 5 trisomy 5p
Camptomelic syndrome
Chromosome 9 trisomy
Triploidy
Partial monosomy
Monosomy 9p
Mucocutaneous lymph node disease
Mucopolysa- ccharidosis iii
Munchausens syndrome
Mucopolysa- ccharidosis iv
Muscle fasciculation
Mucopolysa- ccharidosis, type I
Mucolipidoses
Myxoma
Chromosomal disorder
Karyotype 47,XXX
5p- syndrome
MGA type II
Jacobsen syndrome
3-M Syndrome
47,XYY
Mental retardation
Craniosynostosis
Myelodysplastic syndromes
Trigonocephaly
Trisomy 9
Congenital heart defects
Patau syndrome
Craniofacial dysostosis
Cystic hygroma
Hypotonia
Microcephaly
more...
See also
(16)
Myocardial contusion
Myxoma
Gonadal
The Long Arm
Craniofacial
Craniofacial
Am. J. Med. Genet.
Distal
Sex chromosomes
Genetic counselling
Anaphase lag
Trisomy 21
Prenatal diagnosis
Human height
Mullerian duct
Array CGH
Hormone replacement therapy (menopause)
more...
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