Kosmix
One sec... we're building your guide for
Trisomy 9
Trisomy 9
Overview
Health Providers & Organizations
Main ›
Related in the Kosmos
?
Genetic disorder
Warkany syndrome 2
Chromosome 5q deletion syndrome
Trisomy 22
Trisomy 16
Trichorhin- ophalangeal syndrome
Miller-Dieker syndrome
Pediatrics
Down syndrome
Fragile x syndrome
Genetic disorders
(35)
Trisomy
49 xxxxy syndrome
49, XXXXX
22q11.2 deletion syndrome
47,XYY
47,XYY
Tetrasomy
Tetrasomy 9p
Triple X syndrome
Jacobsen syndrome
Partial trisomy
1p36 deletion syndrome
Trisomy 18
48,xxxx
Chromosomal abnormalities
Monosomy
Patau syndrome
XX gonadal dysgenesis
Cri du chat
Craniofacial dysostosis
Wolf-Hirschhorn syndrome
Turner syndrome
Smith-Magenis syndrome
Carnitine deficiency
Angelman syndrome
Charcot-Marie Tooth Disease
Williams syndrome
Warkany syndrome 2
Chromosome 5q deletion syndrome
Genetic condition
Trisomy 22
Trisomy 16
Trichorhin- ophalangeal syndrome
Miller-Dieker syndrome
Down syndrome
Fragile x syndrome
more...
Diseases and disorders
(41)
Chromosome 9 trisomy
Chromosome 9 trisomy 9p
Chromosome 9 trisomy mosaic
Acute myeloblastic leukemia with maturation
Chromosome 9 tetrasomy 9p
Chromosome 9 tetrasomy 9p
Acute megakaryoblastic leukemia
Acute lymphoblastic leukemia
Congenital hypomyelination
Chromosome 5 trisomy 5p
Camptomelic syndrome
Trisomy 13/18
Cat eye syndrome
Uniparental disomy
Essential thrombocytopenia
Myxoid liposarcoma
Talipes
Cutis laxa
Acute promyelocytic leukemia
Congenital heart defects
Toxoplasmosis
Mental retardation
Rare diseases
Torn meniscus
Trisomy 22
22q11.2 deletion syndrome
47,XYY
Triple X syndrome
Jacobsen syndrome
Partial trisomy
Trisomy 18
Trichorhin- ophalangeal syndrome
48,xxxx
Chromosomal abnormalities
Patau syndrome
Down syndrome
Cri du chat
Craniofacial dysostosis
Carnitine deficiency
Fragile x syndrome
Angelman syndrome
Charcot-Marie Tooth Disease
more...
Cytogenetics
(20)
46,XY
Autosomal
Chromosomal translocation
Chromosome
Chromosomal abnormalities
Chromosomal abnormalities
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Partial trisomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
Syndromes
(16)
Warkany syndrome 2
22q11.2 deletion syndrome
47,XYY
Triple X syndrome
Trisomy 18
Trisomy 18
Miller-Dieker syndrome
Patau syndrome
Down syndrome
Cri du chat
Craniofacial dysostosis
Wolf-Hirschhorn syndrome
Turner syndrome
Smith-Magenis syndrome
Fragile x syndrome
Angelman syndrome
Williams syndrome
more...
Genetics
Chromosomal mosaicism
Chromosomes
Nondisjunction
Genetic disorders
Genetic condition
47,XYY
Chromosomes
(57)
Chromosome 10
Chromosome 11
Chromosome 13
Chromosome 16
Chromosome 18
Chromosome 18
Chromosome 3
Chromosome 4
Chromosome 8
Chromosome 9
Ring chromosome
Short arm
46,XY
AZF1
Allosome
Autosomal
Centromere
Chromatid
Chromomere
Chromosomal abnormalities
Chromosomal inversion
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 12 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Lampbrush chromosome
Marker chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
Y chromosome
more...
See also
(20)
MKL1
RBM15
Abl gene
FOXO1
IgH
IgH
Thoracic vertebrae
Support organization
Telecanthus
Trisomy 21
Craniofacial
Spinal nerve
Prenatal diagnosis
Malformations
Amniocentesis
Psychomotor retardation
Genetic counseling
ICD-O
Dysplasia
Neil J. Gunther
Maternal
more...
more categories...
Health Providers & Organizations
›
Vitals.com
