| 疾病名称 |
别名 |
|
| Lymphoproliferative Syndrome, X-Linked, 1 |
|
Lymphomatoid Papulosis
|
Duncan Disease
|
|
Purtilo Syndrome
|
X-Linked Lymphoproliferative Syndrome
|
|
Xlp
|
X-Linked Lymphoproliferative Disease
|
|
XLP1
|
Lyp
|
|
Lymphoproliferative Disease, X-Linked
|
Xlpd
|
|
X-Linked Lymphoproliferative Disease Due To Sh2d1a Deficiency
|
Ebv Infection, Severe, Susceptibility To
|
|
Ebvs
|
Immunodeficiency 5
|
|
Imd5
|
X-Linked Lymphoproliferative Syndrome 1
|
|
Epstein-Barr Virus Infection, Familial Fatal
|
Ebv Infection, Severe
|
|
Infectious Mononucleosis, Severe
|
Infectious Mononucleosis, Severe, Susceptibility To
|
|
Immunodeficiency, X-Linked Progressive Combined Variable
|
Epstein Barr Virus Infection, Familial Fatal
|
|
X-Linked Progressive Combined Variable Immunodeficiency 5
|
Epstein-Barr Virus-Induced Lymphoproliferative Disease In Males
|
|
Familial Fatal Epstein-Barr Infection
|
Severe Susceptibility To Ebv Infection
|
|
Severe Susceptibility To Infectious Mononucleosis
|
Sap Deficiency
|
|
Sh2d1a/Slam-Associated Protein Deficiency
|
X-Linked Lymphoproliferative Syndrome Type 1
|
|
X-Linked Progressive Combined Variable Immunodeficiency
|
Lymphoproliferative Syndrome, X-Linked
|
|
Sap
|
X-Linked Lymphoproliferative Disorder
|
|
|
| Lymphoproliferative Syndrome |
|
Lymphoproliferative Disorder
|
Lymphoproliferative Disorders
|
|
Lymphoproliferative Disorders, Susceptibility To
|
|
|
| Dysgammaglobulinemia |
|
|
| Hemophagocytic Lymphohistiocytosis |
|
Lymphohistiocytosis, Hemophagocytic
|
Haemophagocytic Syndrome
|
|
Lymphohistiocytosis Hemophagocytic
|
Hemophagocytic Syndrome
|
|
Familial Hemophagocytic Lymphocytosis
|
Histiocytoses Of Mononuclear Phagocytes
|
|
Haemophagocytic Lymphohistiocytosis Nos
|
|
|
| Pfeiffer Syndrome |
|
Infectious Mononucleosis
|
Acs5
|
|
Craniofacial-Skeletal-Dermatologic Dysplasia
|
Acs V
|
|
Noack Syndrome
|
Gammaherpesviral Mononucleosis
|
|
Acrocephalosyndactyly Type 5
|
Pfeiffer Syndrome Type 3
|
|
Acrocephalosyndactyly, Type V
|
Glandular Fever
|
|
Pfeiffer Type Acrocephalosyndactyly
|
Pfeiffer Syndrome Type 2
|
|
Acrocephalosyndactylia Type V
|
Filatov'S Disease
|
|
Monocytic Angina
|
Mononucleosis
|
|
Pfeiffer'S Disease
|
Acsv
|
|
Acrocephalosyndactyly, Type 5
|
Craniofacial-Skeletal-Dermatologic Syndrome
|
|
Pfeiffer Syndrome Type 1
|
Classic Pfeiffer Syndrome
|
|
PS
|
Pfeiffer Syndrome Variant
|
|
Dysplasia, Craniofacial-Skeletal-Dermatologic
|
Pfeiffer
|
|
Kissing Disease
|
Infectious Adenitis
|
|
Pfeiffer Disease
|
|
|
| Selective Immunoglobulin Deficiency Disease |
|
|
| Lymphoma |
|
Lymphoid Cancer
|
Lymphomas
|
|
Lymphoid Cancers
|
Lymphoid Neoplasm
|
|
Lymphoma Nos
|
Nhl - [Non-Hodgkin Lymphoma]
|
|
Non-Hodgkin Lymphoma
|
Non-Hodgkin Lymphoma, Nos
|
|
Non-Hodgkin Malignant Lymphoma Nos
|
|
|
| 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
|
|
|
| Lymphoproliferative Syndrome, X-Linked, 2 |
|
XLP2
|
Xiap Deficiency
|
|
X-Linked Lymphoproliferative Syndrome 2
|
X-Linked Lymphoproliferative Disease Due To Xiap Deficiency
|
|
Xiap-Related Lymphoproliferative Disease, X-Linked
|
X-Linked Lymphoproliferative Syndrome Type 2
|
|
Xiap Deficiency Syndrome
|
|
|
| Autoinflammatory Syndrome |
|
|
| Agammaglobulinemia |
|
Hypogammaglobulinemia
|
Ighm
|
|
Mu Heavy Chain Deficiency
|
Mu-Heavy Chain Disease
|
|
Mu-Hcd
|
Mu-Chain Disease
|
|
|
| Hemophagocytic Lymphohistiocytosis, Familial, 1 |
|
Familial Hemophagocytic Lymphohistiocytosis
|
Fhl
|
|
Familial Erythrophagocytic Lymphohistiocytosis
|
Hemophagocytic Syndrome
|
|
FHL1
|
Hplh1
|
|
Hlh1
|
Fel
|
|
Familial Hemophagocytic Lymphohistiocytosis 1
|
Primary Hemophagocytic Lymphohistiocytosis
|
|
Familial Hlh
|
Hlh
|
|
Familial Hemophagocytic Lymphocytosis
|
Hemophagocytic Lymphohistiocytosis, Familial
|
|
Reticulosis, Familial Histiocytic
|
Hemophagocytic Reticulosis, Familial
|
|
Erythrophagocytic Lymphohistiocytosis, Familial
|
Familial Histiocytic Reticulosis
|
|
Familial Hemophagocytic Histiocytosis
|
Familial Hemophagocytic Reticulosis
|
|
Fhlh
|
Hplh
|
|
Primary Hemophagocytic Hymphohistiocytosis
|
Genetic Hemophagocytic Lymphohistiocytosis
|
|
Hemophagocytic Lymphohistiocytosis
|
Familial Hemophagocytic Lymphohistiocytosis Type 1
|
|
|
| Burkitt Lymphoma |
|
Burkitt'S Lymphoma
|
BL
|
|
Burkitt Lymphoma, Somatic
|
Burkitt Lymphoma/Leukaemia
|
|
Burkitt'S Tumor
|
Burkitt'S Tumor Or Lymphoma
|
|
Malignant Lymphoma, Burkitt'S Type
|
Small Non-Cleaved Cell Lymphoma, Burkitt'S Type
|
|
Small Non-Cleaved Cell Lymphoma
|
Burkitt Tumor
|
|
Burkitts Lymphoma
|
Lymphoma, Small Noncleaved-Cell
|
|
Burkitt Tumour
|
Diffuse Small Noncleaved Malignant Burkitt Lymphoma
|
|
Malignant Burkitt Lymphoma
|
“Burkitt-Like” Lymphoma
|
|
Undifferentiated Burkitt Lymphoma
|
Small Noncleaved Cell Burkitt Lymphoma
|
|
|
| Candidiasis |
|
Systemic Candidiasis
|
Invasive Candidiasis
|
|
Disseminated Candidiasis
|
Systemic Candida Infections
|
|
Candidiasis, Invasive
|
|
|
| Limbic Encephalitis |
|
|
| Meningoencephalitis |
|
Acquired Toxoplasmal Meningoencephalitis
|
Meningoencephalitis Due To Acquired Toxoplasmosis
|
|
Meningoencephalitis Due To Toxoplasmosis
|
Toxoplasma Meningoencephalitis
|
|
|
| Ras-Associated Autoimmune Leukoproliferative Disorder |
|
RALD
|
Autoimmune Lymphoproliferative Syndrome Type 4
|
|
Alps4
|
Autoimmune Lymphoproliferative Syndrome, Type Iv
|
|
Ras-Associated Autoimmune Leukoproliferative Disease
|
Ras-Associated Autoimmune Lymphoproliferative Syndrome Type Iv, Somatic
|
|
Alps Type 4
|
Alps Type Iv
|
|
Autoimmune Lymphoproliferative Syndrome Type Iv
|
Autoimmune Lymphoproliferative Syndrome 4
|
|
|
| Familial Hemophagocytic Lymphohistiocytosis 5 |
|
Fhl5
|
Hlh5
|
|
Hplh5
|
Lymphohistiocytosis, Hemophagocytic, Familial, Type 5
|
|
|
| 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
|
|
|
| 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
|
|
|
| Pancytopenia |
|
|
| Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia |
|
XMEN
|
X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia
|
|
X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia
|
Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia
|
|
Cid Due To Magt1 Deficiency
|
Combined Immunodeficiency Due To Magt1 Deficiency
|
|
X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection An
|
X-Linked Magnesium Deficiency With Epstein-Barr Virus Infection And Neoplasia
|
|
|
| Lymphoproliferative Syndrome 2 |
|
Cd27 Deficiency
|
LPFS2
|
|
Combined Immunodeficiency Due To Cd27 Deficiency
|
Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency
|
|
|
| Cd3zeta Deficiency |
|
|
| Vasculitis |
|
Angiitis
|
Autoimmune Vasculitis
|
|
Systemic Vasculitis
|
Vasculitis, Autoimmune
|
|
|
| Hemophagocytic Lymphohistiocytosis, Familial, 2 |
|
Familial Hemophagocytic Lymphohistiocytosis 2
|
FHL2
|
|
Hplh2
|
Hlh2
|
|
Hemophagocytic Lymphohistiocytosis, Familial, 2, Susceptibility To
|
Lymphohistiocytosis, Hemophagocytic, Familial, Type 2
|
|
|
| Immunodeficiency 14 |
|
Activated Pi3k-Delta Syndrome
|
Apds
|
|
Pasli Disease
|
Imd14
|
|
Senescent T-Cells-Lymphadenopathy-Immunodeficiency Syndrome Due To P110delta-Activating Mutation
|
P110 Delta-Activating Mutation Causing Senescent T Cells, Lymphadenopathy, And Immunodeficiency
|
|
|
| Hemophagocytic Lymphohistiocytosis, Familial, 3 |
|
Familial Hemophagocytic Lymphohistiocytosis 3
|
FHL3
|
|
Hplh3
|
Hlh3
|
|
Lymphohistiocytosis, Hemophagocytic, Familial, Type 3
|
|
|
| Griscelli Syndrome |
|
Chediak-Higashi-Like Syndrome
|
Griscelli-Prunieras Syndrome
|
|
Partial Albinism-Immunodeficiency Syndrome
|
Griscelli Disease
|
|
Gs
|
Hypopigmentation Immunodeficiency Disease
|
|
Partial Albinism With Immunodeficiency
|
Immunodeficiency Syndrome With Hypopigmentation
|
|
Hypopigmentation-Immunodeficiency Disease
|
|
|
| Griscelli Syndrome, Type 2 |
|
Griscelli Syndrome Type 2
|
GS2
|
|
Griscelli Syndrome With Hemophagocytic Syndrome
|
Partial Albinism And Immunodeficiency Syndrome
|
|
Paid Syndrome
|
Hypopigmentation-Immunodeficiency With Or Without Neurologic Impairment Syndrome
|
|
Griscelli-Prunieras Syndrome Type 2
|
Griscelli-Pruniéras Syndrome Type 2
|
|
Griscelli Syndrome 2
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Immunodeficiency 7 |
|
Tcr-Alpha-Beta-Positive T-Cell Deficiency
|
IMD7
|
|
T-Cell Receptor-Alpha/Beta Deficiency
|
Immunodeficiency 7, Tcr-Alpha/Beta Deficient
|
|
Tcr-Alpha/Beta Deficiency
|
Tcr-Alpha-Beta+ T-Cell Deficiency
|
|
T-Cell Receptor Alpha/Beta Deficiency
|
|
|
| B Cell Deficiency |
|
Immunoglobulin Heavy Chain Deficiency
|
B Cell Deficiencies
|
|
Immunoglobulin Heavy Chain Deletion
|
Humoral Immune Defect
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| Lymphoma, Hodgkin, Classic |
|
Hodgkin Lymphoma
|
Hodgkin Disease
|
|
Hodgkin'S Lymphoma
|
Hodgkins Lymphoma
|
|
Classic Hodgkin Lymphoma
|
CHL
|
|
Hodgkin Lymphoma, Susceptibility To
|
Hl
|
|
Hodgkin'S Sarcoma
|
Stage I Subdiaphragmatic Hodgkin Lymphoma
|
|
Stage Ii Subdiaphragmatic Hodgkin Lymphoma
|
Lymphoma, Hodgkin'S
|
|
Classic Hodgkin Disease
|
Hodgkin'S Disease
|
|
Lymphoma, Hodgkin, Susceptibility To
|
Hodgkin'S Disease Of Intrapelvic Lymph Nodes
|
|
Hodgkin'S Disease Of Lymph Nodes Of Inguinal Region And/Or Lower Limb
|
Malignant Lymphogranuloma
|
|
Malignant Lymphogranulomatosis
|
Malignant Hodgkin Lymphoma
|
|
Classical Hodgkin Lymphoma, Type Not Specified
|
|
|
| Chediak-Higashi Syndrome |
|
CHS
|
Chédiak-Higashi Syndrome
|
|
Chediak - Steinbrinck Anomaly
|
Chediak Higashi Syndrome
|
|
Chediak-Steinbrinck-Higashi Syndrome
|
Oculocutaneous Albinism With Leukocyte Defect
|
|
Chediak-Higashi Disease
|
Chediak-Higashi-Steinbrink Syndrome
|
|
|
| Systemic Epstein-Barr Virus Positive T-Cell Lymphoma Of Childhood |
|
Ebv-Positive T-Cell Lymphoproliferative Disorder Of Childhood
|
Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood
|
|
Systemic Ebv-Positive T-Cell Lymphoma Of Childhood
|
Systemic Ebv+ T-Cell Lymphoma Of Childhood
|
|
|
| Aplastic Anemia |
|
Aplastic Anemia, Susceptibility To
|
Anemia Aplastic
|
|
Idiopathic Aplastic Anemia
|
Secondary Aplastic Anemia
|
|
Idiopathic Bone Marrow Failure
|
Aplastic Anemia Idiopathic
|
|
AA
|
Anemia, Aplastic
|
|
Aplastic Anemia, Idiopathic
|
Erythroid Aplasia
|
|
Aa - [Aplastic Anaemia]
|
Haematopoietic Aplasia
|
|
Aleukia Haemorrhagica
|
Anaemia Due To Decreased Red Cell Production
|
|
Aplasia Bone Marrow
|
Aplastic Bone Marrow
|
|
Hypoplastic Anaemia Nos
|
Myeloid Bone Marrow Aplasia
|
|
Pancytopenia
|
Panhaematopenia
|
|
Hypoproliferative Anaemia
|
Medullary Hypoplasia
|
|
Red Blood Cells Hypoplastic Anaemia
|
Panmyelophthisis
|
|
Panhemocytopenia
|
Refractive Hypoproliferative Anaemia
|
|
Toxic Anaemia
|
Toxic Aplastic Anaemia
|
|
Aplastic Anaemia Due To Toxic Cause
|
Idiopathic Aplastic Anaemia Nos
|
|
|
| Acute Hemorrhagic Encephalitis |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hermansky-Pudlak Syndrome |
|
Hps
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
|
|
Hermanski-Pudlak Syndrome
|
Hermansky Pudlak Syndrome
|
|
Platelet Storage Pool Deficiency
|
|
|
| Epidermodysplasia Verruciformis 1 |
|
Epidermodysplasia Verruciformis
|
Epidermodysplasia Verruciformis, Susceptibility To, 1
|
|
Lutz-Lewandowsky Epidermodysplasia Verruciformis
|
EV1
|
|
Lewandowsky-Lutz Syndrome
|
Ev
|
|
|
