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Xyy Syndrome
XYY syndrome
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Klinefelter's syndrome
Overview
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Syndromes
(15)
Warkany syndrome 2
Turner syndrome
22q11.2 deletion syndrome
X-linked mental retardation and macroorchidism
47,XXX
47,XXX
3-M Syndrome
18p deletion syndrome
Patau syndrome
5p- syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
47,XX,+21
4p- syndrome
Trisomy 18
X-linked primary hyperuricemia
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Genetics
(8)
Chromosomes
Mosaicism
48 xxyy syndrome
XX male syndrome
Satellite chromosome
Satellite chromosome
X linked
Nondisjunction
Human chromosomes
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Genetic disorders
(40)
49, XXXXX
49 xxxxy syndrome
48,xxxx
Chromosomal abnormalities
Chromosome 5q deletion syndrome
Chromosome 5q deletion syndrome
Aneuploidy
Isodicentric chromosome 15 syndrome
Trisomy
Trisomy 16
1p36 deletion syndrome
MGA type II
Hyperostosis, cortical, congenital
Trisomy 22
Adrenoleuk- odystrophy
Leukodystrophy, globoid cell
Trisomy 9
Polysomy
Galactosemias
Spinal and bulbar muscular atrophy
5-oxoprolinuria
4-hydroxybutyric aciduria
XX gonadal dysgenesis
Jacobsen syndrome
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Monosomies
Warkany syndrome 2
Turner syndrome
22q11.2 deletion syndrome
X-linked mental retardation and macroorchidism
47,XXX
48 xxyy syndrome
XX male syndrome
18p deletion syndrome
Patau syndrome
5p- syndrome
Hereditary sensory and autonomic neuropathies
47,XX,+21
4p- syndrome
Trisomy 18
X-linked primary hyperuricemia
more...
Diseases and disorders
(51)
Acute myeloblastic leukemia with maturation
Acute megakaryoblastic leukemia
Xeroderma pigmentosum variant type
Acute lymphoblastic leukemia
Supernumerary roots
Supernumerary roots
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
18p syndrome
Encephalitis, arbovirus
Olfaction disorders
X-linked retinoschisis
Intervertebral disk displacement
Polyploid
Rosenthal syndrome
X-linked lymphoproliferative syndrome
Brachial plexus neuropathies
Cat eye syndrome
X-linked hypophosphatemia
Macrodontia (tooth)
Optic neuropathy, ischemic
48,xxxx
Chromosomal abnormalities
Aneuploidy
22q11.2 deletion syndrome
X-linked mental retardation and macroorchidism
47,XXX
XX male syndrome
3-M Syndrome
MGA type II
Hyperostosis, cortical, congenital
Trisomy 22
Patau syndrome
5p- syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Trisomy 9
47,XX,+21
Trisomy 18
Galactosemias
Spinal and bulbar muscular atrophy
Jacobsen syndrome
X-linked primary hyperuricemia
more...
Rare diseases
(8)
49, XXXXX
48,xxxx
Chromosome 5q deletion syndrome
5p- syndrome
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
5-oxoprolinuria
4-hydroxybutyric aciduria
X-linked primary hyperuricemia
more...
Cytogenetics
(20)
Chromosome
Karyotype
Mixoploidy
X chromosome
Aneuploidy
Aneuploidy
Autosome
Chromosomal abnormalities
Chromosomal translocation
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomies
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
more...
Chromosomes
(57)
Centromere
Chromatids
Chromosome 21
Short arm
Small supernumerary marker chromosome
Small supernumerary marker chromosome
Y chromosome
AZF1
Allosome
Autosome
Chromomere
Chromosomal abnormalities
Chromosomal inversion
Chromosomal translocation
Chromosome
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 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
Satellite chromosome
Subtelomere
Syntelic
Telomere
X chromosome
more...
See also
(18)
Sex chromosome
FOXO1
Abl gene
MKL1
Heterochromatin
Heterochromatin
RBM15
IgH
Cusp of carabelli
Chromosome (genetic algorithm)
Xanthoma tuberosum
Theophilus Painter
Diploid
Inner enamel epithelium
Telophase II
Cementoenamel junction
Thoracic vertebrae
Klinefelter's syndrome
Microtubules
more...
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