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Trisomy 22
Trisomy 22
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Genetic disorder
Warkany syndrome 2
Chromosome 5q deletion syndrome
Trisomy 9
Trisomy 16
Miller-Dieker syndrome
Trichorhin- ophalangeal syndrome
Diseases and disorders
Syndromes
Cubitus valgus
Hypoplastic
Genetic disorders
(34)
Trisomy
Trisomy 13
Trisomy 18
49 xxxxy syndrome
49, XXXXX
49, XXXXX
Chromosomal abnormalities
Down syndrome
22q11.2 deletion syndrome
Partial trisomy
Distal Trisomy 10q
Tetrasomy
Turner syndrome
48,xxxx
Philadelphia chromosome
47,XYY
Jacobsen syndrome
Phelan-McDermid syndrome
Monosomy
Triple X syndrome
Charcot-Marie Tooth Disease
XX gonadal dysgenesis
Cri du chat
Angelman syndrome
Craniofacial dysostosis
Microphthalmia
Wolf-Hirschhorn syndrome
Isodicentric 15
Smith-Magenis syndrome
Warkany syndrome 2
Chromosome 5q deletion syndrome
Trisomy 9
Trisomy 16
Miller-Dieker syndrome
Trichorhin- ophalangeal syndrome
more...
Cytogenetics
(20)
Autosomal
Chromosome
Fluorescence in situ hybridization
Karyotype
Robertsonian translocation
Robertsonian translocation
Translocations
Uniparental disomy
X chromosomes
Chromosomal abnormalities
Colcemid
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Partial trisomy
Ploidy
Pseudoautosomal region
Synapsis
Tetrasomy
Trisomy
more...
Syndromes
(17)
Trisomy 13
Trisomy 18
49 xxxxy syndrome
Down syndrome
Warkany syndrome 2
Warkany syndrome 2
22q11.2 deletion syndrome
Distal Trisomy 10q
Turner syndrome
47,XYY
Phelan-McDermid syndrome
Triple X syndrome
Miller-Dieker syndrome
Cri du chat
Angelman syndrome
Craniofacial dysostosis
Wolf-Hirschhorn syndrome
Smith-Magenis syndrome
more...
Genetics
Chromosomes
Mosaicism
Human chromosomes
Nondisjunction
Genetic disorders
47,XYY
Cytogenetics
Congenital disorders
Cat eye syndrome
Malformations
Genetic disorders
Blood disorders
Acute myeloblastic leukemia with maturation
Acute lymphoblastic leukemia
Essential thrombocytopenia
Chromosome 5q deletion syndrome
Types of cancer
Acute megakaryoblastic leukemia
Follicular lymphoma
Myxoid liposarcoma
Acute lymphoblastic leukemia
Pregnancy tests
(14)
Amniocentesis
Chorionic villus sampling
Nuchal translucency
Prenatal diagnosis
3D ultrasound
3D ultrasound
Abderhalden reaction
Aschheim-Zondek test
Baby Gender Mentor
Gravindex
HCG pregnancy strip test
Obstetric ultrasonography
Percutaneous umbilical cord blood sampling
Pregnancy test
Proteogenix
more...
Chromosomes
(54)
Centromere
Chromosome 11
Chromosome 15
Chromosome 21
Chromosome 22
Chromosome 22
Chromosome 3
Chromosome 4
Isochromosome
Marker chromosome
Pericentric inversion
Ring chromosome
Short arm
AZF1
Allosome
Autosomal
Chromatid
Chromomere
Chromosomal abnormalities
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 18 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 5 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Karyotype
Lampbrush chromosome
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
Translocations
X chromosomes
Y chromosome
more...
Medical condition
(37)
Chromosome 22 trisomy mosaic
Chromosome 22 trisomy
Chromosome 9 trisomy
Chromosome 5 trisomy 5p
Congenital hypomyelination
Congenital hypomyelination
Chromosome 9 tetrasomy 9p
Camptomelic syndrome
Emanuel syndrome
Chromosome 22 ring
Chromosome 18 ring
Chromosome 14 trisomy mosaic
Trisomy 13
Trisomy 18
49 xxxxy syndrome
Chromosomal abnormalities
Down syndrome
Acute myeloblastic leukemia with maturation
22q11.2 deletion syndrome
Partial trisomy
Trisomy 9
Acute megakaryoblastic leukemia
Cat eye syndrome
Acute lymphoblastic leukemia
48,xxxx
47,XYY
Jacobsen syndrome
Triple X syndrome
Uniparental disomy
Charcot-Marie Tooth Disease
Trichorhin- ophalangeal syndrome
Cri du chat
Angelman syndrome
Craniofacial dysostosis
Microphthalmia
Follicular lymphoma
Essential thrombocytopenia
Myxoid liposarcoma
more...
See also
(19)
Trisomy 21
FOXO1
Abl gene
MKL1
RBM15
RBM15
IgH
Maternal age
Confined placental mosaicism
Thoracic nerves
ICD-O
Acrocentric chromosome
Beta HCG
Human chromosome
Sex chromosome
Brushfield spots
Meiotic
Telecanthus
Thoracic vertebrae
Estriol
more...
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