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Philadelphia Chromosome
Philadelphia chromosome
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Genetic disorders
(19)
Chromosome 5q deletion syndrome
49 xxxxy syndrome
49, XXXXX
Chromosomal abnormalities
Warkany syndrome 2
Warkany syndrome 2
22q11.2 deletion syndrome
Trisomy 16
47,XYY
Trisomy 22
Jacobsen syndrome
48,xxxx
Miller-Dieker syndrome
Monosomies
Trisomy 9
Triple X syndrome
Turner syndrome
Klinefelter
Tetrasomy
Extra chromosome
more...
Blood disorders
(128)
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia
Acute myeloid leukemia
Acute promyelocytic leukemia
Chronic myeloid leukemia
Chronic neutrophilic leukemia
Hematology
Leukemic
Mast cell leukemia
Myeloid sarcoma
Acquired hemolytic anemia
Acute myeloid dendritic cell leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
Agranulocytosis
Alpha-thalassemia
Amyloid purpura
Analbuminaemia
Anaplastic large cell lymphoma
Anemia
Anemia of chronic disease
Anemia of prematurity
Angioimmunoblastic T-cell lymphoma
Antiphospholipid syndrome
Aplastic anemia
Atransferrinemia
Autoimmune hemolytic anemia
Autoimmune neutropenia
B symptoms
Bernard-Soulier syndrome
Beta-thalassemia
Bisalbuminemia
Blood hammer
Cavernous sinus thrombosis
Chemothera- py-induced neutropenia
Chromosome 5q deletion syndrome
Congenital amegakaryocytic thrombocytopenia
Congenital dyserythropoietic anemia
Congenital hemolytic anemia
Contaminated haemophilia blood products
Cyclic neutropenia
Deaths from blood disease
Delta-thalassemia
Diamond-Blackfan anemia
Drug-induced autoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia
Enteropath- y-associated T-cell lymphoma
Eosinopenia
Essential thrombocytosis
Evans syndrome
Familial dysfibrinogenemia
Glanzmann's thrombasthenia
Haemophilia
Haemophilia A
Haemophilia B
Haemophilia C
Haemorrhagic and haematological disorders of fetus and newborn
Hairy cell leukemia
Harris platelet syndrome
Hematological malignancy
Hemoglobin variants
Hemoglobinemia
Hemolytic anemia
Hemolytic disease of the newborn
Hemolytic disease of the newborn (ABO)
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hemophagocytic lymphohistiocytosis
Hepatosplenic T-cell lymphoma
Hereditary elliptocytosis
Hereditary pyropoikilocytosis
Hereditary spherocytosis
Hodgkin's lymphoma
Hypersegmented neutrophil
Hypochromic anemia
Hypoprothrombinemia
Idiopathic thrombocytopenic purpura
Laminopathy
Large granular lymphocytic leukemia
Leukopenia
Lindsay Tribunal
List of hemophilia organizations
Loxoscelism
Lymphocytopenia
Lymphoma
Macrocytic anemia
Mantle cell lymphoma
May-Hegglin anomaly
Megaloblastic anemia
Methemoglobinemia
Minimally differentiated acute myeloblastic leukemia
Monoclonal B-cell lymphocytosis
Monoclonal gammopathy of undetermined significance
Myelophthisic anemia
Neonatal alloimmune thrombocytopenia
Neutropenia
Nodular lymphocyte predominant Hodgkin's lymphoma
Non-Hodgkin lymphoma
Paroxysmal cold hemoglobinuria
Pel-Ebstein fever
Plummer-Vinson syndrome
Polycythemia vera
Primary effusion lymphoma
Protein S deficiency
Pseudo gray platelet syndrome
Quebec Platelet Disorder
Refractory anemia
Rh disease
Richter's transformation
Scott syndrome
Sickle cell trait
Sickle-cell disease
Spherocytosis
Splenic marginal zone lymphoma
T-cell prolymphocytic leukemia
Thalassemia
Thrombocytopenia
Thrombocytosis
Triosephosphate isomerase deficiency
Vaso-occlusive crisis
Von Willebrand disease
Waldenström's macroglobulinemia
Warm autoimmune hemolytic anemia
Wiskott-Aldrich syndrome
Working Formulation
more...
Genetic disorder
Chromosome 5q deletion syndrome
Warkany syndrome 2
Trisomy 16
Trisomy 22
Miller-Dieker syndrome
Trisomy 9
Chromosomes
(57)
Autosomes
Chromosomal translocation
Chromosome
Chromosome 22
Chromosome 9
Chromosome 9
Derivative chromosome
G banding
Isochromosome
Karyotype
Marker chromosome
Ring chromosome
X chromosome
Y chromosome
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 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Dicentric chromosome
Dyad (biology)
Human β-globin locus
Inchrosil
Lampbrush chromosome
Locus (genetics)
Personalized medicine
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
more...
Types of cancer
(10)
Acute megakaryoblastic leukemia
Myxoid liposarcoma
Chronic lymphocytic leukemia
Acute lymphoblastic leukemia
Acute eosinophilic leukemia
Acute eosinophilic leukemia
Leukemic
Acute monocytic leukemia
Mast cell leukemia
Myeloid sarcoma
Acute promyelocytic leukemia
more...
Tyrosine kinase inhibitors
(15)
Bosutinib
Imatinib
Nilotinib
Sprycel
Axitinib
Axitinib
Cediranib
Erlotinib
Gefitinib
Lapatinib
Lestaurtinib
Semaxanib
Sunitinib
Toceranib
Vandetanib
Vatalanib
more...
Oncology
Accelerated phase chronic myelogenous leukemia
Acute myeloblastic leukemia
Malignancy
Stem cell transplantation
Acute myeloblastic leukemia with maturation
Myxoid liposarcoma
Chronic lymphocytic leukemia
Cytogenetics
(20)
Chromosome number
Fluorescence in situ hybridization
Autosomes
Chromosomal abnormalities
Chromosomal translocation
Chromosomal translocation
Chromosome
Colcemid
Extra chromosome
Fragile sites
Germ plasm
Homologous chromosome
Karyotype
Monosomies
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
Hematology
(10)
Acute panmyelosis with myelofibrosis
Bone marrow biopsy
Hematologic disease
White blood cells
Myelodysplastic syndromes
Myelodysplastic syndromes
Auer rods
Leukemic
Mast cell leukemia
Myeloid sarcoma
Stem cell transplantation
more...
Medicine
Diseases and disorders
Refractory anemia with excess of blasts
Lymphoid
Chronic eosinophilic leukemia
Miller-Dieker syndrome
Leukemia
(30)
Acute basophilic leukemia
Myelocytic leukemia
Accelerated phase chronic myelogenous leukemia
Acute eosinophilic leukemia
Acute erythroid leukemia
Acute erythroid leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Acute myeloid leukemia
Antileukemic drug
B-cell leukemia
B-cell prolymphocytic leukemia
Chronic lymphocytic leukemia
Chronic myeloid leukemia
Chronic myelomonocytic leukemia
Chronic neutrophilic leukemia
Hairy cell leukemia
Juvenile myelomonocytic leukemia
Large granular lymphocytic leukemia
Lymphoid leukemia
Minimal residual disease
Minimally differentiated acute myeloblastic leukemia
Monocytic leukemia
Myelomonocyte
Plasma cell leukemia
Precursor B acute lymphoblastic leukemia/lymphoma
Prolymphocytic leukemia
T-cell leukemia
T-cell prolymphocytic leukemia
more...
Diseases and disorders
(26)
Refractory cytopenia with multilineage dysplasia
Acute biphenotypic leukaemia
Cat eye syndrome
Chronic myeloid leukemia
Acute lymphoblastic leukemia
Acute lymphoblastic leukemia
Acute myeloblastic leukemia with maturation
Acute megakaryoblastic leukemia
Chromosomal abnormalities
Leukemic
22q11.2 deletion syndrome
Acute monocytic leukemia
47,XYY
Trisomy 22
Hematologic disease
Jacobsen syndrome
48,xxxx
Myxoid liposarcoma
Myelocytic leukemia
Acute myeloid leukemia
Myelodysplastic syndromes
Trisomy 9
Triple X syndrome
Klinefelter
Extra chromosome
Acute promyelocytic leukemia
Chronic lymphocytic leukemia
more...
See also
(20)
Abl gene
Myeloid
BCR gene
Mast-cell sarcoma
Chemical Markup Language
Chemical Markup Language
Tyrosine kinase
MKL1
RBM15
Myeloid dendritic cell
Bcr-abl fusion protein
CFU-Eos
CFU-Mast
FOXO1
Blood cells
Cells
Granulocytes
IgH
Human chromosome
Fusion genes
Thoracic vertebrae
more...
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