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22q11.2 Deletion Syndrome
22q11.2 deletion syndrome
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Genetic disorders
(41)
Spondyloep- imetaphyseal dysplasia, Strudwick type
Charcot-Marie-Tooth disease, type 4
Cayler syndrome
Very long-chain acyl coenzyme A dehydrogenase deficiency
Microdeletion
Microdeletion
47 xyy syndrome
1p36 deletion syndrome
49 xxxxy syndrome
Trisomy
Williams syndrome
Warkany syndrome 2
Kniest dysplasia
22q13
Trisomy 22
Otospondyl- omegaepiphyseal dysplasia
Spinal and bulbar muscular atrophy
Prader Willi syndrome
X-linked sideroblastic anemia
Aneuploidy
49, XXXXX
48,xxxx
Turner syndrome
SADDAN
Spondyloepiphyseal dysplasia congenita
Chromosomal abnormalities
Triple X syndrome
Smith-Magenis syndrome
Cornelia de Lange syndrome
Wolf-Hirschhorn syndrome
X-linked severe combined immunodeficiency
Tetrasomy
Trisomy 9
Fragile x syndrome
Crouzon syndrome
Cri du chat
Alexander disease
Monosomy
Stickler syndrome
Canavan disease
Patau syndrome
Noonan syndrome
more...
Syndromes
(20)
Sotos syndrome
Syndrome
Charge syndrome
47 xyy syndrome
49 xxxxy syndrome
49 xxxxy syndrome
Williams syndrome
Warkany syndrome 2
22q13
Prader Willi syndrome
Turner syndrome
Triple X syndrome
Smith-Magenis syndrome
Cornelia de Lange syndrome
Wolf-Hirschhorn syndrome
Fragile x syndrome
Crouzon syndrome
Cri du chat
Stickler syndrome
Patau syndrome
Noonan syndrome
more...
Medical condition
(42)
Chromosome 22q deletion
Ehlers-danlos syndrome dermatosparaxis type
Tetralogy of fallot
Alzheimer disease type 2
Cat eye syndrome
Cat eye syndrome
Atelosteogenesis type 2
Hypoparathyroidism
Myotonic dystrophy type 2
Heart defects
Hypocalcemia
Interrupted aortic arch
Cleft palate
Craniosynostosis
Psychotic disorders
Uniparental disomy
Feeding difficulties
Spondyloep- imetaphyseal dysplasia, Strudwick type
Charcot-Marie-Tooth disease, type 4
Cayler syndrome
47 xyy syndrome
49 xxxxy syndrome
Kniest dysplasia
Spinal and bulbar muscular atrophy
Prader Willi syndrome
X-linked sideroblastic anemia
Aneuploidy
48,xxxx
Spondyloepiphyseal dysplasia congenita
Chromosomal abnormalities
Triple X syndrome
Sotos syndrome
Cornelia de Lange syndrome
Trisomy 9
Fragile x syndrome
Crouzon syndrome
Cri du chat
Alexander disease
Stickler syndrome
Charge syndrome
Canavan disease
Patau syndrome
Noonan syndrome
more...
Medical terms
Diseases and disorders
Hypoplasia
Neuronopathy
Chromosomes
(54)
Autosomal
Balanced translocation
Chromosome
Chromosome 22
Subtelomere
Subtelomere
AZF1
Allosome
Centromere
Chromatid
Chromomere
Chromosomal abnormalities
Chromosomal inversion
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 11 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 18 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 3 (human)
Chromosome 4 (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
Isochromosome
Karyotype
Lampbrush chromosome
Locus (genetics)
Marker chromosome
Proline-Rich Coiled Coil 1
Ring chromosome
Satellite chromosome
Small supernumerary marker chromosome
Syntelic
Telomere
X chromosome
Y chromosome
more...
Congenital disorders
Congenital heart disease
Congenital bilateral absence of vas deferens
Malformation
Genetic disorders
Cat eye syndrome
Cleft palate
Genetics
Medical genetics
Low copy repeats
Copy number
Cytogenetic
Genetic disorders
Microdeletion
47 xyy syndrome
Parathyroid disorders
Parathyroid glands
Hyperparathyroidism
Hypoparathyroidism
Parathyroid disease
Secondary hyperparathyroidism
Tertiary hyperparathyroidism
Cytogenetics
(20)
Aneuploidy
Autosomal
Balanced translocation
Chromosomal abnormalities
Chromosome
Chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Karyotype
Monosomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
See also
(20)
TBX1
American Journal of Human Genetics
Human Molecular Genetics
Fourth pharyngeal pouch
Thymic hypoplasia
Thymic hypoplasia
Multiplex Ligation-dependent Probe Amplification
Thymus
delete (C++)
Trisomy 21
Human chromosome
Prenatal diagnosis
Array CGH
Voxel based morphometry
Autosomal dominant
Am. J. Med. Genet. A
Craniofacial
Pulmonary artery
Marine Life Protection Act
Prefrontal cortex
Short stature
more...
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