| Diseases |
Alias |
|
| Immunoglobulin A Deficiency 2 |
|
IGAD2
|
Immunoglobulin A, Selective Deficiency Of, Taci-Related
|
|
Iga, Selective Deficiency Of, Taci-Related
|
Iga, Selective Deficiency Of, Taci Related
|
|
Immunoglobulin A, Selective Deficiency Of, Taci Related
|
Immunoglobulin A Deficiency, Type 2
|
|
|
| Immunodeficiency, Common Variable, 2 |
|
CVID2
|
Antibody Deficiency Due To Taci Defect
|
|
Hypogammaglobulinemia Due To Taci Deficiency
|
Common Variable Immunodeficiency 2
|
|
Immunodeficiency, Variable, Common, Type 2
|
|
|
| Common Variable Immunodeficiency |
|
Cvid
|
Common Variable Agammaglobulinemia
|
|
Common Variable Immune Deficiency
|
Acquired Hypogammaglobulinemia
|
|
Hypogamma-Globulinemia, Acquired
|
Idiopathic Immunoglobulin Deficiency
|
|
Primary Antibody Deficiency
|
Primary Hypogammaglobulinemia
|
|
Acquired Agammaglobulinemia
|
Sporadic Hypogammaglobulinemia
|
|
Common Variable Hypogamma-Globulinemia
|
Immunoglobulin Deficiency, Late-Onset
|
|
Common Variable Hypogammaglobulinemia
|
Immunodeficiency, Common Variable
|
|
|
| Immunodeficiency, Common Variable, 1 |
|
CVID1
|
Antibody Deficiency Due To Icos Defect
|
|
Icos Deficiency
|
Common Variable Immunodeficiency 1
|
|
Immunodeficiency, Variable, Common, Type 1
|
|
|
| Immunoglobulin Alpha Deficiency |
|
Iga Deficiency
|
Gamma-A-Globulin Deficiency
|
|
Immunoglobulin A Deficiency
|
|
|
| Primary Agammaglobulinemia |
|
Immunoglobulin Deficiency
|
Antibody Deficiency Syndrome
|
|
Antibody
|
Antibody Deficiency
|
|
Gammaglobulin Deficiency
|
Antibody Deficiency With Near-Normal Immunoglobulins Or With Hyperimmunoglobulinaemia
|
|
Immunoglobulin Deficiency With Near-Normal Immunoglobins
|
Immunoglobulin Deficiency With Hyperimmunoglobulinaemia
|
|
Antibody Immunodeficiency With Hyperimmunoglobulinaemia
|
Antibody Deficiency With Hyperimmunoglobulinaemia
|
|
|
| Smith-Magenis Syndrome |
|
SMS
|
Chromosome 17p11.2 Deletion Syndrome
|
|
17p11.2 Microdeletion Syndrome
|
17p11.2 Monosomy
|
|
Chromosome 17p Deletion Syndrome
|
Del(17)
|
|
P11.2
|
17p- Syndrome
|
|
Deletion 17p Syndrome
|
Partial Monosomy 17p
|
|
|
| Selective Ige Deficiency Disease |
|
Selective Immunoglobulin E Deficiency
|
Selective Ige Immunodeficiency
|
|
|
| Transient Hypogammaglobulinemia Of Infancy |
|
Immunoglobulin Maturational Delay
|
Thi - [Transient Hypogammaglobulinaemia Of Infancy]
|
|
|
| Cd40 Ligand Deficiency |
|
X-Linked Hyper Igm Syndrome
|
Hyperimmunoglobulin M Syndrome
|
|
Higm1
|
Hyper-Igm Syndrome Type 1
|
|
X-Linked Hyper-Igm Syndrome
|
Xhigm
|
|
Higmx-1
|
X-Linked Hyper-Igm Immunodeficiency
|
|
Hyper-Igm Syndrome 1
|
Immunodeficiency With Hyper-Igm, Type 1
|
|
Hyper-Igm Syndrome Due To Cd40 Ligand Deficiency
|
Hyper-Igm Syndrome Due To Cd40l Deficiency
|
|
Hyper-Igm Immunodeficiency Syndrome
|
Hyper-Igm Immunodeficiency Syndrome, Type 1
|
|
|
| Transient Hypogammaglobulinemia |
|
|
| Macroglobulinemia |
|
Primary Macroglobulinemia
|
Waldenstrom Macroglobulinemia
|
|
|
| B Cell Deficiency |
|
Immunoglobulin Heavy Chain Deficiency
|
B Cell Deficiencies
|
|
Immunoglobulin Heavy Chain Deletion
|
Humoral Immune Defect
|
|
|
| Autoimmune Disease |
|
Autoimmune Diseases
|
Autoimmune Hypersensitivity Disease
|
|
Hypersensitivity Reaction Type Ii Disease
|
Type Ii Hypersensitivity Reaction Disease
|
|
|
| Selective Igg Deficiency Disease |
|
Igg Deficiency
|
Immunoglobin G Subclass Deficiency
|
|
Selective Deficiency Of Igg
|
Selective Igg Immunodeficiency
|
|
Selective Immunoglobulin G Deficiency
|
Selective Immunoglobulin G Subclass Deficiency
|
|
|
| Selective Immunoglobulin Deficiency Disease |
|
|
| Immunoglobulin A Deficiency 1 |
|
Immunoglobulin A Deficiency
|
Selective Iga Deficiency Disease
|
|
Selective Immunoglobulin A Deficiency
|
IGAD1
|
|
Immunoglobulin A, Selective Deficiency Of
|
Iga, Selective Deficiency Of
|
|
Gamma-A-Globulin, Selective Deficiency Of
|
Selective Iga Immunodeficiency
|
|
Selective Iga Deficiency
|
Iga Deficiency Selective
|
|
|
| Good Syndrome |
|
Immunodeficiency With Thymoma
|
Thymoma-Immunodeficiency Syndrome
|
|
Thymoma With Hypogammaglobulinemia
|
Thymoma Immunodeficiency
|
|
|
| Evans' Syndrome |
|
Evans Syndrome
|
Autoimmune Hemolytic Anemia And Autoimmune Thrombocytopenia
|
|
Evan Syndrome
|
Immune Pancytopenia
|
|
Evan'S Syndrome
|
|
|
| Dysgammaglobulinemia |
|
|
| Immunodeficiency With Hyper-Igm, Type 1 |
|
Immunodeficiency, X-Linked, With Hyper-Igm
|
Hyper Igm Syndrome
|
|
HIGM1
|
Xhim
|
|
Hyper-Igm Syndrome
|
Higm
|
|
Hyper-Igm Syndrome 1
|
Immunodeficiency 3
|
|
Imd3
|
Immunodeficiency With Hyper-Igm
|
|
Immunodeficiency With Hyper Igm Type 1
|
Ihis
|
|
X-Linked Hyper Igm Syndrome
|
Hyper-Igm Immunodeficiency, X-Linked
|
|
Hyper Igm Immunodeficiency, X-Linked
|
Hyper Igm Syndrome 1
|
|
X-Linked Immunodeficiency With Hyper-Igm 1
|
Immunodeficiency, With Hyper Igm
|
|
Immunodeficiency, With Hyper Igm, Type 1
|
Hyper-Igm Immunodeficiency Syndrome, Type 1
|
|
Hyperimmunoglobulin M Syndrome
|
|
|
| Immunodeficiency With Hyper-Igm, Type 3 |
|
HIGM3
|
Immunodeficiency With Hyper Igm Type 3
|
|
Hyper-Igm Syndrome Type 3
|
Hyper-Igm Syndrome 3
|
|
Hyper-Igm Syndrome Due To Cd40 Deficiency
|
Cd40 Deficiency
|
|
Type 3 Hyper-Igm Immunodeficiency
|
Hyper Igm Syndrome 3
|
|
Immunodeficiency With Hyper-Igm 3
|
Hyper-Igm Immunodeficiency Type 3
|
|
Immunodeficiency, With Hyper Igm, Type 3
|
Hyper-Igm Immunodeficiency Syndrome, Type 3
|
|
|
| Immunodeficiency With Hyper-Igm, Type 5 |
|
HIGM5
|
Hyper-Igm Syndrome 5
|
|
Immunodeficiency With Hyper Igm Type 5
|
Hyper-Igm Syndrome Type 5
|
|
Hyper-Igm Syndrome Due To Ung Deficiency
|
Hyper-Igm Syndrome Due To Uracil N-Glycosylase
|
|
Immunodeficiency With Hyper Igm, Type 5
|
Hyper Igm Syndrome 5
|
|
Immunodeficiency With Hyper-Igm 5
|
Hyper-Igm Immunodeficiency Type 5
|
|
Immunodeficiency, With Hyper Igm, Type 5
|
Hyper-Igm Immunodeficiency Syndrome, Type 5
|
|
|
| Immunodeficiency With Hyper-Igm, Type 2 |
|
HIGM2
|
Hyper-Igm Syndrome Type 2
|
|
Hyper-Igm Syndrome 2
|
Immunodeficiency With Hyper-Igm Type 2
|
|
Activation-Induced Cytidine Deaminase Deficiency
|
Aid Deficiency
|
|
Immunodeficiency With Hyper Igm Type 2
|
Hyper Igm Syndrome 2
|
|
Immunodeficiency With Hyper-Igm 2
|
Hyper-Igm Immunodeficiency Type 2
|
|
Immunodeficiency, With Hyper Igm, Type 2
|
Hyper-Igm Immunodeficiency Syndrome, Type 2
|
|
|
| Lymphoid Interstitial Pneumonia |
|
Lymphocytic Interstitial Pneumonia
|
Lip Disease
|
|
Lip Diseases
|
LIP
|
|
Disease Of Lips
|
|
|
| Immune Deficiency Disease |
|
Immunodeficiency
|
Primary Immunodeficiency
|
|
Primary Immunodeficiency Disease
|
Immunologic Deficiency Syndromes
|
|
Hypoimmunity
|
Immune Deficiency Disorder
|
|
Immunodeficiency Syndrome
|
Immune Disorder
|
|
Primary Immune Deficiency Disorder
|
Immune System Diseases
|
|
Human Immunodeficiency Virus Infection
|
Hiv - [Human Immunodeficiency Virus Infection]
|
|
Hiv Positive Nos
|
Hiv Disease
|
|
Acquired Immune Deficiency Syndrome-Related Complex
|
Aids-Like Syndrome
|
|
Aids-Related Complex Nos
|
Arc - [Aids-Related Complex]
|
|
Immunodeficiency Due To Human Immunodeficiency Virus Infection
|
Unspecified Human Immunodeficiency Virus Disease
|
|
Hiv Disease Nos
|
Human Immunodeficiency Virus Positive Nos
|
|
Hiv Nos
|
Deficiency Of Complement Initial Pathway
|
|
Deficiency Of Complement Terminal Pathway
|
Cfdd - [Complement Factor D Deficiency]
|
|
Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency
|
Nonfamilial Hypogammaglobulinaemia
|
|
Common Variable Immune Deficiency
|
Nonfamilial Agammaglobulinaemia
|
|
Common Variable Agammaglobulinaemia
|
Agammaglobulinaemia Nos
|
|
Agammaglobulinaemia Antibody Deficiency Syndrome
|
Hypogammaglobulinaemia Antibody Deficiency Syndrome
|
|
Acquired Agammaglobulinaemia Nos
|
Hypogammaglobulinaemia Nos
|
|
Hyper Igm
|
|
|
| Agammaglobulinemia, X-Linked |
|
X-Linked Agammaglobulinemia
|
XLA
|
|
Bruton Type Agammaglobulinemia
|
Bruton'S Agammaglobulinemia
|
|
Bruton-Type Agammaglobulinemia
|
Agmx1
|
|
Imd1
|
Agammaglobulinemia, X-Linked 1
|
|
Btk-Deficiency
|
Agammaglobulinemia
|
|
Hypogammaglobulinemia
|
Agammaglobulinemia, X-Linked, Type 1
|
|
Immunodeficiency 1
|
Bruton Agammaglobulinemia Tyrosine Kinase Deficiency
|
|
Bruton Disease
|
Bruton'S Agammaglobulinaemia
|
|
Bruton'S Sex-Linked Agammaglobulinemia
|
Bruton'S Type Agammaglobulinemia
|
|
Btk Deficiency
|
Agammaglobulinemia, Btk
|
|
Agammaglobulinemia, Bruton Tyrosine Kinase
|
Congenital Agammaglobulinemia
|
|
Immunodeficiency Type 1
|
X-Linked Agammaglobulinemia Type 1
|
|
|
| Follicular Lymphoma |
|
Lymphoma, Follicular
|
Lymphoma Follicular
|
|
Brill-Symmers' Disease
|
Large Cell Follicular Non-Hodgkin Lymphoma
|
|
Diffuse Follicle Centre Lymphoma
|
Diffuse Follicular Lymphoma Nos
|
|
Follicular Nodular Non-Hodgkin Lymphoma, Unspecified
|
Follicular Large Cell Cleaved Or Noncleaved Lymphoma
|
|
Large Cell Follicular Noncleaved Lymphoma
|
Follicular Lymphoma With Or Without Diffuse Areas
|
|
Histiocytic Follicular Lymphoma
|
Histiocytic Nodular Lymphoma
|
|
Histiocytic Nodular Malignant Lymphoma
|
Large Cell Follicular Lymphoma
|
|
Large Cell Noncleaved Follicular Lymphoma
|
Large Cell Noncleaved Follicular Malignant Lymphoma
|
|
Nodular Reticulum Cell Sarcoma
|
Noncleaved Follicular Lymphoma
|
|
|
| Lymphoma, Non-Hodgkin, Familial |
|
Non-Hodgkin Lymphoma
|
Lymphoma, Non-Hodgkin
|
|
NHL
|
Lymphoma, Non-Hodgkin, Somatic
|
|
Lymphoma, Follicular, Somatic
|
Familial Non-Hodgkin Lymphoma
|
|
Lymphoma Non-Hodgkins
|
Follicular Lymphoma, Somatic
|
|
Lymphosarcoma
|
Non-Hodgkins Lymphoma
|
|
|
| Anemia, Autoimmune Hemolytic |
|
Autoimmune Hemolytic Anemia
|
Idiopathic Autoimmune Hemolytic Anemia
|
|
Immuno-Hemolytic Anemia
|
Anemia, Hemolytic, Autoimmune
|
|
Autoimmune Haemolytic Anaemia
|
Autoimmune Hemolytic Anaemia
|
|
Acquired Autoimmune Hemolytic Anemia
|
Anemia Hemolytic Autoimmune
|
|
Familial Auto-Immune Hemolytic Anemia
|
Aha
|
|
Aiha
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Lymphoproliferative Syndrome 2 |
|
Cd27 Deficiency
|
LPFS2
|
|
Combined Immunodeficiency Due To Cd27 Deficiency
|
Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency
|
|
|
| Primary Thrombocytopenia |
|
|
| Thrombocytopenia Due To Platelet Alloimmunization |
|
Immune Thrombocytopenia
|
Autoimmune Thrombocytopenia
|
|
Immune Thrombocytopenic Purpura
|
Itp
|
|
Auto-Immune Thrombocytopenia
|
Thrombocytopenia Due To Immune Destruction
|
|
Autoimmune Thrombocytopenic Purpura
|
Idiopathic Thrombocytopenic Purpura
|
|
Werlhof Disease
|
|
|
| Myeloma, Multiple |
|
Multiple Myeloma
|
Plasma Cell Myeloma
|
|
Kahler Disease
|
Myelomatosis
|
|
Medullary Plasmacytoma
|
Multiple Myeloma, Resistance To
|
|
Myeloma
|
Plasma Cell Dyscrasia
|
|
Kahler'S Disease
|
Multiple Myeloma, Susceptibility To
|
|
Myeloma - Multiple
|
Kahler-Bozzolo Disease
|
|
Plasma Cell Myelomas
|
MM
|
|
Plasma Cell Neoplasm
|
Primary Systemic Amyloidosis
|
|
Primary Amyloidosis
|
Immunoglobulin Deposition Disease
|
|
Plasmacytic Myeloma
|
Multiple Myelomata
|
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
|
Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
| Leukemia, Chronic Lymphocytic |
|
Chronic Lymphocytic Leukemia
|
B-Cell Chronic Lymphocytic Leukemia
|
|
CLL
|
B-Cell Chronic Lymphoid Leukemia
|
|
Chronic Lymphatic Leukemia
|
Chronic Lymphocytic Leukaemia
|
|
Lymphoplasmacytic Leukemia
|
Small Lymphocytic Lymphoma
|
|
Leukemia, Chronic Lymphatic
|
B-Cell Chronic Lymphocytic Leukaemia
|
|
Chronic Lymphatic Leukaemia
|
Lymphoplasmacytic Leukaemia
|
|
B Cell Chronic Lymphocytic Leukemia
|
Chronic B-Cell Lymphocytic Leukemia
|
|
Leukemia, Lymphocytic, Chronic
|
B-Cll
|
|
Chronic Lymphoid Leukemia
|
Leukemia Lymphocytic Chronic
|
|
Lymphoma Small Lymphocytic
|
Leukemia, Lymphocytic, Chronic, B-Cell
|
|
|
| Combined Immunodeficiency |
|
Combined T Cell And B Cell Immunodeficiency
|
Congenital Combined Immunodeficiency
|
|
Syndrome With Combined Immunodeficiency
|
Combined T And B Cell Immunodeficiency
|
|
Combined Immunity Deficiency
|
Combined Immunodeficiency Syndrome
|
|
Combined T-Cell And B-Cell Immunodeficiency
|
Lymphopenic Agammaglobulinaemia
|
|
|
| Potocki-Shaffer Syndrome |
|
Proximal 11p Deletion Syndrome
|
Chromosome 11p11.2 Deletion Syndrome
|
|
Pss
|
11p11.2 Deletion
|
|
P11pds
|
Defect11 Syndrome
|
|
Deletion Of Chromosome 11p11.2
|
POSHS
|
|
|
| Autoimmune Lymphoproliferative Syndrome |
|
ALPS
|
Canale-Smith Syndrome
|
|
Autoimmune Lymphoproliferative Syndrome, Type Ia
|
Autoimmune Lymphoproliferative Syndrome, Type Ib
|
|
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
|
Css
|
|
Autoimmune Lymphoproliferative Syndrome, Type 1b
|
Autoimmune Lymphoproliferative Syndrome, Type 1a
|
|
Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
|
Fas Deficiency
|
|
Autoimmune Lymphoproliferative Syndrome 1a
|
ALPS1A
|
|
Autoimmune Lymphoproliferative Syndrome Type Ia
|
Autoimmune Lymphoproliferative Syndrome 1b
|
|
ALPS1B
|
Autoimmune Lymphoproliferative Syndrome Type Ib
|
|
|
| Omenn Syndrome |
|
Histiocytic Medullary Reticulosis
|
Severe Combined Immunodeficiency With Hypereosinophilia
|
|
Combined Immunodeficiency With Hypereosinophilia
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
|
Reticuloendotheliosis Familial With Eosinophilia
|
Familial Reticuloendotheliosis
|
|
Omenn'S Syndrome
|
OS
|
|
Malignant Histiocytosis
|
|
|
