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X-linked Lymphoproliferative Syndrome
X-linked lymphoproliferative syndrome
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Noninfectious immunodeficiency-related cutaneous conditions
(25)
22q11.2 deletion syndrome
Bare lymphocyte syndrome
Common variable immunodeficiency
IgM deficiency
Immunodeficiency with hyper-IgM
Immunodeficiency with hyper-IgM
Myeloperoxidase deficiency
Nezelof syndrome
Omenn syndrome
Purine nucleoside phosphorylase deficiency
Severe combined immunodeficiency
WHIM syndrome
Wiskott-aldrich syndrome
X linked agammaglobulinemia
Cartilage–hair hypoplasia
Chediak–Higashi syndrome
Chronic granulomatous disease
Complement deficiency
Graft-versus-host disease
Griscelli syndrome
Hyperimmunoglobulin E syndrome
Leukocyte adhesion molecule deficiency
Neutropenia
Selective immunoglobulin A deficiency
Thymoma with immunodeficiency
X-linked hyper-immu- noglobulin M syndrome
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Diseases and disorders
(72)
Glycogen storage disease type iib
Purtilo syndrome
Complement 2 deficiency
Lymphohistiocytosis
MASA syndrome
MASA syndrome
Zap70 deficiency
Reticular dysgenesis
Acute biphenotypic leukemia
X-linked sideroblastic anemia
X-linked hypophosphatemia
Mevalonic aciduria
Metabolic syndrome
Adenosine deaminase deficiency
Lymphoproliferative
Heavy chain disease
Xeroderma pigmentosum variant type
Becker's muscular dystrophy
Hyper IgM syndrome
Infectious mononucleosis
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Lipid storage disorder
X-linked mental retardation and macroorchidism
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Immunoproliferative
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Sly syndrome
Pyruvate dehydrogenase deficiency
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Alport syndrome
Intervertebral disk displacement
Rosenthal syndrome
Hemophagocytic lymphohistiocytosis
Focal dermal hypoplasia
Centronuclear myopathy
X-linked retinoschisis
Angioedema
Galactosemias
Brachial plexus neuropathies
Hurler-Scheie Syndrome
XXY syndrome
Leukemia
Optic neuropathy, ischemic
Combined immunodeficiencies
Spondyloepiphyseal dysplasia
Androgen insensitivity syndrome
Barth syndrome
X-linked ichthyosis
Autoimmune lymphoproliferative syndrome
Hypogammag- lobulinemia
Omenn syndrome
Nezelof syndrome
IgM deficiency
Myeloperoxidase deficiency
Purine nucleoside phosphorylase deficiency
22q11.2 deletion syndrome
Wiskott-aldrich syndrome
X linked agammaglobulinemia
Severe combined immunodeficiency
Common variable immunodeficiency
Bare lymphocyte syndrome
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Immune system
Hyper IgM Syndrome Type 1
ICF syndrome
Immune disorders
Myeloperoxidase deficiency
Hyper IgM syndrome
Autoimmune lymphoproliferative syndrome
Immunology
Hyper IgM Syndrome Type 1
ICF syndrome
Myeloperoxidase deficiency
Hyper IgM syndrome
Autoimmune lymphoproliferative syndrome
Lysosomal storage diseases
(40)
Mucolipidosis II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type iib
Glycoproteinosis
Hunter syndrome
Hurler-Scheie Syndrome
Leukodystrophy, globoid cell
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Inborn errors of metabolism
(8)
Glycogen storage disease type iib
Mevalonic aciduria
Adenosine deaminase deficiency
Lipid storage disorder
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
Sly syndrome
Galactosemias
X-linked ichthyosis
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Rare diseases
(14)
XXXXX syndrome
Lelis syndrome
Glycogen storage disease type iib
Omenn syndrome
Zap70 deficiency
Zap70 deficiency
ICF syndrome
WHIM syndrome
Purine nucleoside phosphorylase deficiency
Adenosine deaminase deficiency
Lipid storage disorder
Leukodystrophy, globoid cell
Sly syndrome
Wiskott-aldrich syndrome
Severe combined immunodeficiency
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Syndromes
(17)
XO syndrome
McLeod syndrome
Omenn syndrome
Nezelof syndrome
ICF syndrome
ICF syndrome
WHIM syndrome
Metabolic syndrome
X-linked mental retardation and macroorchidism
22q11.2 deletion syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Sly syndrome
Alport syndrome
Hurler-Scheie Syndrome
XXY syndrome
Androgen insensitivity syndrome
Lelis syndrome
more...
Immune system disorders
(63)
Immunodeficiency
22q11.2 deletion syndrome
Aagenaes syndrome
Alternative names for chronic fatigue syndrome
Antinuclear antibodies
Antinuclear antibodies
Asplenia
Atopy
Autoimmune diseases
Autosplenectomy
Castleman's disease
Chronic fatigue syndrome
Chronic fatigue syndrome treatment
Chronic granulomatous disease
Clinical descriptions of chronic fatigue syndrome
Controversies related to chronic fatigue syndrome
Cryofibrinogenemia
Cultural references to chronic fatigue syndrome
Cytokine release syndrome
Cytokine storm
Dennie-Morgan fold
Endocrine paraneoplastic syndrome
Erdheim–Chester disease
Extracutaneous mastocytoma
Familial Mediterranean fever
Food allergies
Food allergy
Graft-versus-host disease
Gulf War syndrome
HIV/AIDS
HLA-B27
History of chronic fatigue syndrome
Hyperimmunoglobulin E syndrome
Hypersensitivity
Idiopathic CD4+ lymphocytopenia
Immune reconstitution inflammatory syndrome
Immune-mediated disease
Kimura disease
Leukocyte adhesion deficiency
List of people with chronic fatigue syndrome
Lymphocytopenia
Lymphoproliferative
Mastocytosis
Mortimer's disease
Multiple Myeloma Research Foundation
Myeloperoxidase deficiency
Opportunistic infection
Oral allergy syndrome
Paraneoplastic syndrome
Pathophysiology of chronic fatigue syndrome
Pityriasis lichenoides chronica
Pityriasis lichenoides et varioliformis acuta
Seabather's eruption
Selective immunoglobulin A deficiency
Systemic autoimmune diseases
Systemic inflammatory response syndrome
Transplant rejection
Type I hypersensitivity
Type II hypersensitivity
Type III hypersensitivity
Type IV hypersensitivity
Wiskott-aldrich syndrome
X linked agammaglobulinemia
Zap70 deficiency
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Immunodeficiency
(14)
X-scid
Adenosine deaminase deficiency
Bare lymphocyte syndrome
Common variable immunodeficiency
Complement deficiency
Complement deficiency
HIV
HIV/AIDS
ICF syndrome
Idiopathic CD4+ lymphocytopenia
Immunodeficiency (Acquired immunodeficiency)
Nezelof syndrome
Primary immunodeficiency
Severe combined immunodeficiency
Severe combined immunodeficiency (non-human)
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See also
(20)
X linked
SH2D1A
Hematological malignancy
Refractory anemia with excess blasts in transformation
Aicardi syndrome
Aicardi syndrome
Adrenoleuk- odystrophy
Alternative names for chronic fatigue syndrome (Chronic Epstein-Barr virus)
Simpson-Go- labi-Behmel syndrome
Mendel, johann
Escuela Bella Vista
B't X
AIFM1
BIRC4
X-linked recessive
Juvenile Myelomonocytic Leukemia (JMML)
Xanthoma tuberosum
MAP3K7IP1
Letters by alphabet
KAL1
Spectral karyotype
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