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Trisomy 18
Trisomy 18
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Types & Stages
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Related in the Kosmos
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Syndromes
(10)
Trisomy 13
Down syndrome
Turner syndrome
Cri du chat
Trisomy 8
Trisomy 8
Xyy syndrome
Distal Trisomy 10q
Treacher Collins syndrome
Russell-Silver syndrome
Triple X syndrome
more...
Genetic disorders
(20)
Partial trisomy
Trisomy
Chromosomal disorder
Trisomy 9
Monosomy
Monosomy
Trisomy 16
Smith-lemli-opitz syndrome
Trisomy 22
Polydactyly
Microcephaly
Genetic condition
Trisomy 13
Down syndrome
Turner syndrome
Cri du chat
Trisomy 8
Xyy syndrome
Distal Trisomy 10q
Treacher Collins syndrome
Triple X syndrome
more...
Diseases and disorders
(49)
Trisomy 13/18
Tricuspid atresia
Persistent truncus arteriosus
Tracheoesophageal fistula
Uniparental disomy
Uniparental disomy
Triploidy
Micrognathia
Turner-like syndrome
Hyperlipop- roteinemia type I
Trichiniasis
Tuberculosis
Transposition of great vessels
Omphalocele
Neonatal hyperbilirubinemia
Chromosome 14 trisomy mosaic
Chromosome 5 trisomy 5p
Chromosome 9 trisomy mosaic
Diaphragmatic hernia
Chromosome 22 trisomy mosaic
Talipes
Choroid plexus cysts
Horseshoe kidney
Chromosome 18 monosomy 18p
Chromosome 9 trisomy
Chromosome 7 partial monosomy 7p
Chromosomal triplication
Mental retardation
Skeletal dysplasia
Chromosome 6 partial trisomy 6q
Chromosome 18 tetrasomy 18p
Anencephaly
Chromosome 9 trisomy 9p
Intrauterine growth restriction
Chromosome 11 partial trisomy 11q
Chromosome 15 distal trisomy 15q
Congenital heart defects
Chromosome 4 partial trisomy distal 4q
Partial trisomy
Trisomy 13
Chromosomal disorder
Down syndrome
Trisomy 9
Syndromes
Cri du chat
Xyy syndrome
Trisomy 22
Polydactyly
Microcephaly
Triple X syndrome
more...
Cytogenetics
(20)
Autosomes
Balanced translocation
Chromosomal
Karyotype
Chromosomal disorder
Chromosomal disorder
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...
Genetics
Mosaicism
Chromosome 18 (human)
Chromosomes
Nondisjunction
Genetic disorders
Xyy syndrome
Genetic condition
Chromosomes
(57)
Chromatids
Chromosome 10
Chromosome 13
Chromosome 4
Ring chromosome
Ring chromosome
Short arm
AZF1
Allosome
Autosomes
Balanced translocation
Centromere
Chromomere
Chromosomal
Chromosomal disorder
Chromosomal inversion
Chromosome 1 (human)
Chromosome 11 (human)
Chromosome 12 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 18
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 3 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
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...
Congenital heart disease
(34)
Acyanotic heart defect
Atrial septal defect
Baffle (medical)
Children's Heart Foundation
Congenital heart defects
Congenital heart defects
Cor triatriatum
Cyanotic heart defect
Double aortic arch
Double inlet left ventricle
Double outlet right ventricle
Ebstein's anomaly
Fontan procedure
GUCH
Hypoplastic left heart syndrome
Interrupted aortic arch
Kawashima procedure
Noncompaction cardiomyopathy
Norwood procedure
Overriding aorta
Patent ductus arteriosus
Persistent truncus arteriosus
Pulmonary atresia
Sakati-Nyh- an-Tisdale syndrome
Scimitar syndrome
Sinus venosus atrial septal defect
Taussig-Bing syndrome
Tetralogy of Fallot
Total anomalous pulmonary venous connection
Transposition of great vessels
Tricuspid atresia
Uhl anomaly
Ventricular septal defect
dextro-Tra- nsposition of the great arteries
levo-Transposition of the great arteries
more...
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...
Obstetrics
(10)
Triple test
Neural tube defects
Alpha fetoprotein
Polyhydramnios
Amniotic fluid
Amniotic fluid
Nuchal translucency
Amniocentesis
Prenatal diagnosis
Chorionic villus sampling
Intrauterine growth restriction
more...
Pregnancy
Advanced maternal age
First trimester
Nuchal translucency
Amniotic fluid
Congenital disorders
(11)
Holoprosencephaly
Malformations
Cyclopia
Genetic disorders
Neural tube defects
Neural tube defects
Omphalocele
Talipes
Polydactyly
Horseshoe kidney
Microcephaly
Anencephaly
more...
Symptoms
(14)
Low set ears
Coloboma
Diastasis recti
Hydronephrosis
Inguinal hernia
Inguinal hernia
Pectus carinatum
Polycystic kidney disease
Umbilical hernia
Mental retardation
Atrial septal defect
Patent ductus arteriosus
Ventricular septal defect
Anencephaly
Congenital heart defects
more...
See also
(20)
Trisomy 21
Quad screen
Maternal age
Umbilical artery
Tongue inflammation
Tongue inflammation
Transtentorial herniation
Support organization
Craniofacial
Genetic counselling
Palpebral fissures
99 balloons
Ventriculomegaly
Sex chromosome
Ductus venosus
Chromosome studies
Singleplay video game
Translocation
Www.trisomy.org
Www.trisomy18.org
Am. J. Med. Genet.
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