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49, Xxxxx
49, XXXXX
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Related in the Kosmos
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Rare diseases
Chromosome 5q deletion syndrome
48 xxxx syndrome
5-oxoprolinuria
4-hydroxybutyric aciduria
5p- syndrome
Genetic disorders
(25)
49 xxxxy syndrome
Chromosomal abnormalities
22q11.2 deletion syndrome
Warkany syndrome 2
Karyotype 47,XXX
Karyotype 47,XXX
47,XYY
MGA type II
Penta X syndrome
Trisomy 16
Trisomy 22
18p deletion syndrome
48 xxyy syndrome
4p- syndrome
Turner syndrome
Klinefelter syndrome
Jacobsen syndrome
Miller-Dieker syndrome
Partial monosomy
Philadelphia chromosome
Tetrasomy
Chromosome 5q deletion syndrome
48 xxxx syndrome
5-oxoprolinuria
4-hydroxybutyric aciduria
5p- syndrome
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Cytogenetics
(20)
Karyotype
Mixoploidy
X chromosomes
Autosome
Chromosomal abnormalities
Chromosomal abnormalities
Chromosomal translocation
Chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Partial monosomy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
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Blood disorders
Acute myeloblastic leukemia with maturation
Acute lymphoblastic leukemia
Acute promyelocytic leukemia
Chromosome 5q deletion syndrome
Genetic disorder
Chromosome 5q deletion syndrome
Warkany syndrome 2
Trisomy 16
Trisomy 22
48 xxyy syndrome
Miller-Dieker syndrome
Types of cancer
Acute megakaryoblastic leukemia
Myxoid liposarcoma
AIDS-related lymphoma
Acute lymphoblastic leukemia
Acute promyelocytic leukemia
Medicine
Diseases and disorders
Lymphoid
Penta X syndrome
Miller-Dieker syndrome
Gene
FOXO1
MKL1
RBM15
Diseases and disorders
(21)
18p syndrome
5th disease
Intellectual disability
Hematologic disease
Chromosomal abnormalities
Chromosomal abnormalities
Acute myeloblastic leukemia with maturation
22q11.2 deletion syndrome
Acute megakaryoblastic leukemia
48 xxxx syndrome
Karyotype 47,XXX
47,XYY
Acute lymphoblastic leukemia
MGA type II
3-M Syndrome
Trisomy 22
5p- syndrome
Klinefelter syndrome
Jacobsen syndrome
Partial monosomy
Myxoid liposarcoma
Acute promyelocytic leukemia
more...
See also
(14)
Abl gene
IgH
3-M Syndrome
Thoracic nerves
Mosaicism
Mosaicism
Spinal nerve
Myeloid
Sex chromosomes
ICD-O
Xxx xxx
Marginal zone
Congenital malformations
X inactivation
Marion
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