| 疾病名称 |
别名 |
|
| Lymphoproliferative Syndrome 2 |
|
Cd27 Deficiency
|
LPFS2
|
|
Combined Immunodeficiency Due To Cd27 Deficiency
|
Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency
|
|
|
| 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
|
|
|
| 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
|
|
|
| Combined T And B Cell Immunodeficiency |
|
|
| Lymphoproliferative Syndrome |
|
Lymphoproliferative Disorder
|
Lymphoproliferative Disorders
|
|
Lymphoproliferative Disorders, Susceptibility To
|
|
|
| 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
|
|
|
| Pars Planitis |
|
Posterior Cyclitis
|
Vitritis
|
|
Intermediate Uveitis
|
Peripheral Retinal Inflammation
|
|
Uveitis, Intermediate
|
|
|
| Tetanus |
|
Lockjaw
|
Clostridial Tetanus
|
|
Infection Due To Clostridium Tetani
|
Lock-Jaw
|
|
|
| Myelitis |
|
Spinal Cord Inflammation Nos
|
Radiculomyelitis Nos
|
|
Myeloradiculitis
|
|
|
| Neuromyelitis Optica |
|
Devic Disease
|
Devic Syndrome
|
|
Neuromyelitis Optica Spectrum Disorder
|
Devic'S Disease
|
|
Devic'S Syndrome
|
Devic'S Neuromyelitis Optica
|
|
Nmo
|
Nmo Spectrum Disorder
|
|
Neuromyelitis Optica Spectrum Disorders
|
Devic Neuromyelitis Optica
|
|
Optic-Spinal Ms
|
Opticospinal Ms
|
|
Nmosd
|
Opticospinal Multiple Sclerosis
|
|
Devic
|
Ophthalmoneuromyelitis
|
|
Optic Neuromyelitis
|
Optic Neuroencephalomyelopathy
|
|
Nmo - [Neuromyelitis Optica]
|
Optic Neuritis With Demyelination
|
|
|
| Hemophagocytic Lymphohistiocytosis |
|
Lymphohistiocytosis, Hemophagocytic
|
Haemophagocytic Syndrome
|
|
Lymphohistiocytosis Hemophagocytic
|
Hemophagocytic Syndrome
|
|
Familial Hemophagocytic Lymphocytosis
|
Histiocytoses Of Mononuclear Phagocytes
|
|
Haemophagocytic Lymphohistiocytosis Nos
|
|
|
| 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
|
|
|
| Cryoglobulinemia |
|
|
| 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
|
|
|
| Granulomatosis With Polyangiitis |
|
GPA
|
Wegener Granulomatosis
|
|
Wegener Granulomatosis, Formerly
|
Midline Granulomatosis
|
|
Wg, Formerly
|
Necrotizing Respiratory Granulomatosis
|
|
Wg
|
Wegeners Granulomatosis
|
|
Pauci-Immune Glomerulonephritis Associated With Granulomatosis With Polyangiitis
|
|
|
| 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 Of Infancy |
|
Immunoglobulin Maturational Delay
|
Thi - [Transient Hypogammaglobulinaemia Of Infancy]
|
|
|
| Macroglobulinemia |
|
Primary Macroglobulinemia
|
Waldenstrom Macroglobulinemia
|
|
|
| Transient Hypogammaglobulinemia |
|
|
| B Cell Deficiency |
|
Immunoglobulin Heavy Chain Deficiency
|
B Cell Deficiencies
|
|
Immunoglobulin Heavy Chain Deletion
|
Humoral Immune Defect
|
|
|
| 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
|
|
|
| Digeorge Syndrome |
|
Chromosome 22q11.2 Deletion Syndrome
|
DGS
|
|
Hypoplasia Of Thymus And Parathyroids
|
Third And Fourth Pharyngeal Pouch Syndrome
|
|
22q11.2 Deletion Syndrome
|
Digeorge Sequence
|
|
Digeorge'S Syndrome
|
Pharyngeal Pouch Syndrome
|
|
Di-George Syndrome
|
Shprintzen Syndrome
|
|
|
| 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
|
|
|
| Severe Combined Immunodeficiency |
|
Scid
|
Severe Combined Immunodeficiency Disease
|
|
Combined T And B Cell Inborn Immunodeficiency
|
Immunodeficiency, Severe Combined
|
|
Scid - [Severe Combined Immunodeficiencies]
|
|
|
| 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
|
|
|
| Plasmacytoma |
|
Solitary Plasmacytoma
|
Solitary Myeloma
|
|
Myeloma - Solitary
|
Myeloma, Solitary
|
|
Plasmacytoma - Category
|
Solitary Osseous Plasmacytoma
|
|
Solitary Plasmacytoma Without Mention Of Remission
|
Localised Malignant Plasma Cell Tumour Nos
|
|
Plasmacytoma Nos
|
|
|
| Igg4-Related Disease |
|
Multifocal Fibrosclerosis
|
Igg4-Related Sclerosing Disease
|
|
Igg4-Related Systemic Disease
|
Immunoglobulin G4-Related Sclerosing Disease
|
|
Hyper-Igg4 Disease
|
Igg4-Associated Disease
|
|
Igg4-Positive Multiorgan Lymphoproliferative Syndrome
|
Igg4-Related Autoimmune Disease
|
|
Igg4-Related Systemic Sclerosing Disease
|
Igg4-Syndrome
|
|
Multifocal Idiopathic Fibrosclerosis
|
Systemic Igg4-Related Plasmacytic Syndrome
|
|
Systemic Igg4-Related Sclerosing Syndrome
|
Mediastinal Fibrosis, Familial
|
|
Retroperitoneal Fibrosis, Familial
|
Igg4-Rd
|
|
|
| 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 16 |
|
Combined Immunodeficiency Due To Ox40 Deficiency
|
IMD16
|
|
Ox40 Deficiency
|
Combined Immunodeficiency With Childhood-Onset Kaposi Sarcoma
|
|
Combined Immunodeficiency With Impaired Immunity To Hhv-8
|
Combined Immunodeficiency With Impaired Immunity To Human Herpes Virus 8
|
|
Immunodeficiency, Type 16
|
|
|
| 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]
|
|
|
| Immunodeficiency With Hyper-Igm, Type 4 |
|
HIGM4
|
Hyper-Igm Syndrome Type 4
|
|
Immunodeficiency With Hyper-Igm Type 4
|
Hyper-Igm Syndrome 4
|
|
Immunodeficiency With Hyper Igm Type 4
|
Hyper Igm Syndrome 4
|
|
Immunodeficiency, With Hyper Igm, Type 4
|
|
|
| Lymphoid Interstitial Pneumonia |
|
Lymphocytic Interstitial Pneumonia
|
Lip Disease
|
|
Lip Diseases
|
LIP
|
|
Disease Of Lips
|
|
|
| Immunoglobulin Alpha Deficiency |
|
Iga Deficiency
|
Gamma-A-Globulin Deficiency
|
|
Immunoglobulin A Deficiency
|
|
|
| Chickenpox |
|
|
| T Cell Deficiency |
|
T Cell Immunodeficiency
|
T Lymphocyte Deficiency
|
|
T Lymphocyte Immunodeficiency
|
T-Lymphocyte Deficiency
|
|
|
| Selective Immunoglobulin Deficiency Disease |
|
|
| Multiple Sclerosis |
|
MS
|
Multiple Sclerosis, Susceptibility To
|
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
| 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
|
|
|
| Lymphoplasmacytic Lymphoma |
|
Waldenstrom Macroglobulinemia
|
Malignant Lymphoma - Lymphoplasmacytic
|
|
Waldenström Macroglobulinaemia
|
Waldenström Macroglobulinaemia Without Mention Of Remission
|
|
Idiopathic Macroglobulinaemia
|
Primary Macroglobulinaemia
|
|
|
| Monoclonal Gammopathy Of Uncertain Significance |
|
Monoclonal Gammopathy Of Undetermined Significance
|
Mgus
|
|
Mgus - [Monoclonal Gammopathy Of Undetermined Significance]
|
Monoclonal Gammopathy Nos
|
|
Iga Gammopathy
|
Monoclonal Gammoglobulinopathy
|
|
|
| Asymmetric Motor Neuropathy |
|
|
| 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
|
|
|
| Autoimmune Disease Of Exocrine System |
|
|
| Sarcoidosis 1 |
|
Sarcoidosis
|
Boeck Sarcoid
|
|
Besnier-Boeck-Schaumann Disease
|
SS1
|
|
Sarcoidosis, Susceptibility To, 1
|
Lymphogranulomatosis
|
|
Hodgkin Disease
|
Boeck'S Disease
|
|
Boeck'S Sarcoid
|
Schaumann'S Disease Or Syndrome
|
|
Hutchinson-Boeck Disease Or Syndrome
|
|
|
| Hypersensitivity Reaction Type Iv Disease |
|
Immunoproliferative Disorders
|
Immunoproliferative Disease
|
|
|
| Herpangina |
|
|
| 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
|
|
|
| Pediculus Humanus Corporis Infestation |
|
Body Louse Infestation
|
Pediculus Corporis
|
|
Pediculus Humanus Infestation
|
|
|
| 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]
|
|
|
| Primary Bacterial Infectious Disease |
|
|
| Refractory Plasma Cell Neoplasm |
|
|
| Disseminated Eosinophilic Collagen Disease |
|
|
| Bronchiectasis 1 |
|
|
| 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
|
|
|
| Solid Adenocarcinoma With Mucin Production |
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
