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Jacobsen Syndrome
Jacobsen syndrome
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Genetic disorders
(35)
49 xxxxy syndrome
49, XXXXX
Chromosome 5q deletion syndrome
22q11.2 deletion syndrome
Isodicentric chromosome 15 syndrome
Isodicentric chromosome 15 syndrome
Warkany syndrome 2
Turner syndrome
48,xxxx
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
47,XYY
Trisomy 16
Johanson blizzard syndrome
Glutaricaciduria
Trisomy 22
Triple-x females
Juvenile gout
Partial monosomy
Chromosomal abnormalities
VATER syndrome
Galactosemias
Juvenile Spinal Muscular Atrophy
Multiple hereditary exostoses
Monosomy
Jarcho-levin syndrome
Tetrasomy
Thrombocytopenia absent radius
Jervell Lange-Nielsen syndrome
Ablepharon macrostomia syndrome
Miller-Dieker syndrome
Trisomy
Shwachman syndrome
Joubert syndrome
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Diseases and disorders
(56)
Acute myeloblastic leukemia with maturation
Acute megakaryoblastic leukemia
Fetofetal transfusion
Acute lymphoblastic leukemia
Jansen type metaphyseal chondrodysplasia
Jansen type metaphyseal chondrodysplasia
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Craniofrontonasal dysplasia
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Floating harbor syndrome
Juberg hayward syndrome
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Juberg marsidi syndrome
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Optic neuropathy, ischemic
Jackknife convulsion
Jejunal atresia
Joseph disease
Opitz syndrome
Juvenile rheumatoid arthritis
Myxoid liposarcoma
Trigonocephaly
Ollier disease
Pick disease of the brain
Acute promyelocytic leukemia
22q11.2 deletion syndrome
48,xxxx
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
47,XYY
Glutaricaciduria
Trisomy 22
Triple-x females
Juvenile gout
Partial monosomy
Chromosomal abnormalities
VATER syndrome
Galactosemias
Juvenile Spinal Muscular Atrophy
Multiple hereditary exostoses
Jarcho-levin syndrome
Thrombocytopenia absent radius
Ablepharon macrostomia syndrome
Shwachman syndrome
Joubert syndrome
more...
Rare diseases
(9)
49, XXXXX
Chromosome 5q deletion syndrome
48,xxxx
Leukodystrophy, globoid cell
Johanson blizzard syndrome
Johanson blizzard syndrome
Juvenile gout
Multiple hereditary exostoses
Jervell Lange-Nielsen syndrome
Ablepharon macrostomia syndrome
more...
Blood disorders
Acute myeloblastic leukemia with maturation
Chromosome 5q deletion syndrome
Acute lymphoblastic leukemia
Acute promyelocytic leukemia
Genetic disorder
Chromosome 5q deletion syndrome
Warkany syndrome 2
Trisomy 16
Trisomy 22
Ablepharon macrostomia syndrome
Miller-Dieker syndrome
Cytogenetics
(20)
Karyotype
Autosome
Chromosomal abnormalities
Chromosomal translocation
Chromosome
Chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Partial monosomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
Chromosomes
(57)
Centromere
Chromatids
Chromosome 11
Satellite chromosome
Short arm
Short arm
Small supernumerary marker chromosome
Subtelomeric
AZF1
Allosome
Autosome
Chromomere
Chromosomal abnormalities
Chromosomal inversion
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 18 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 3 (human)
Chromosome 4 (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
Ring chromosome
Syntelic
Telomere
X chromosome
Y chromosome
more...
See also
(20)
Congenital disorders
FOXO1
Abl gene
MKL1
RBM15
RBM15
IgH
Chromosome (genetic algorithm)
Jumping Frenchmen
Theophilus Painter
Thoracic vertebrae
Trousseau syndrome
Diploid
Array CGH
Hallervorden-spatz syndrome
Microtubules
Metaphase
Jessica Kingsley Publishers
Histones
Lymphoid
Spinal nerve
more...
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