| 疾病名称 |
别名 |
|
| Lig4 Syndrome |
|
Dna Ligase Iv Deficiency
|
Ligase 4 Syndrome
|
|
LIG4S
|
|
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| Myeloma, Multiple |
|
Multiple Myeloma
|
Plasma Cell Myeloma
|
|
Kahler Disease
|
Myelomatosis
|
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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
|
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Plasmacytic Myeloma
|
Multiple Myelomata
|
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
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Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
| Dubowitz Syndrome |
|
Dubowitz'S Syndrome
|
Dwarfism-Eczema-Peculiar Facies Syndrome
|
|
Intrauterine Growth Restriction, Short Stature, Microcephaly, Mild Intellectual Disability With Behavior Problems, Eczema, And Unusual And Distinctive Faci
|
|
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| Plasma Cell Neoplasm |
|
Plasma Cell Dyscrasia
|
Paraproteinemias
|
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Plasma Cell Tumour
|
Plasmacytic Tumor
|
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Multiple Myeloma
|
Plasmacytoma
|
|
Plasma Cell Tumours
|
Plasma Cells Dyscrasia
|
|
|
| Severe Combined Immunodeficiency |
|
Scid
|
Severe Combined Immunodeficiency Disease
|
|
Combined T And B Cell Inborn Immunodeficiency
|
Immunodeficiency, Severe Combined
|
|
Scid - [Severe Combined Immunodeficiencies]
|
|
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| Omenn Syndrome |
|
Histiocytic Medullary Reticulosis
|
Severe Combined Immunodeficiency With Hypereosinophilia
|
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Combined Immunodeficiency With Hypereosinophilia
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
|
Reticuloendotheliosis Familial With Eosinophilia
|
Familial Reticuloendotheliosis
|
|
Omenn'S Syndrome
|
OS
|
|
Malignant Histiocytosis
|
|
|
| Nijmegen Breakage Syndrome |
|
Berlin Breakage Syndrome
|
NBS
|
|
Microcephaly, Normal Intelligence And Immunodeficiency
|
Ataxia-Telangiectasia Variant
|
|
Ataxia-Telangiectasia Variant V1
|
Seemanova Syndrome Ii
|
|
Immunodeficiency-Microcephaly-Chromosomal Instability Syndrome
|
Seemanova Syndrome Type 2
|
|
At-V1
|
Microcephaly With Normal Intelligence, Immunodeficiency, And Lymphoreticular Malignancies
|
|
Nonsyndromal Microcephaly, Autosomal Recessive, With Normal Intelligence
|
Immunodeficiency, Microcephaly, And Chromosomal Instability
|
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Microcephaly-Immunodeficiency-Lymphoreticuloma Syndrome
|
Microcephaly Immunodeficiency Lymphoreticuloma
|
|
Microcephaly With Normal Intelligence Immunodeficiency And Lymphoreticular Malignancies
|
Nonsyndromal Microcephaly Autosomal Recessive With Normal Intelligence
|
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Seemanova Syndrome 2
|
Ataxia-Telangiectasia Variant 1
|
|
Seemanova Syndrome
|
At V1
|
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Ataxia-Telangiectasia, Variant 1
|
Microcephaly-Immunodeficiency-Lymphoid Malignancy Syndrome
|
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V-At
|
Ataxia Telangiectasia Variant V1
|
|
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| Combined Immunodeficiency |
|
Combined T Cell And B Cell Immunodeficiency
|
Congenital Combined Immunodeficiency
|
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Syndrome With Combined Immunodeficiency
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Combined T And B Cell Immunodeficiency
|
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Combined Immunity Deficiency
|
Combined Immunodeficiency Syndrome
|
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Combined T-Cell And B-Cell Immunodeficiency
|
Lymphopenic Agammaglobulinaemia
|
|
|
| Seckel Syndrome |
|
Microcephalic Primordial Dwarfism
|
Bird-Headed Dwarfism
|
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Harper'S Syndrome
|
Virchow-Seckel Dwarfism
|
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Nanocephalic Dwarfism
|
Sckl
|
|
Seckel-Type Dwarfism
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
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Microcephalic
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Nanocephaly
|
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Congenital Microcephaly
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Brain Hypoplasia
|
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Brain Nondevelopment
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Cephalic Hypoplasia
|
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Undeveloped Cerebrum
|
Undeveloped Brain
|
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Micrencephalon
|
Micrencephaly
|
|
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| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
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Fanconi'S Anemia
|
Fanconi Anaemia
|
|
Fanconi'S Anaemia
|
Fanconi Hypoplastic Anemia
|
|
Estren-Dameshek Variant Of Fanconi Anemia
|
Estren-Dameshek Variant Of Fanconi Pancytopenia
|
|
Fanconi Anemia Estren-Dameshek Variant
|
Fanconis Anemia
|
|
|
| Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation |
|
Severe Combined Immunodeficiency, Athabascan Type
|
Severe Combined Immunodeficiency Due To Dclre1c Deficiency
|
|
Rs-Scid
|
Scid, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive, With Sensitivity To Ionizing Radiation
|
|
Scid Due To Artemis Deficiency
|
Scid Due To Dclre1c Deficiency
|
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Scid, Athabascan Type
|
Scid, Athabaskan Type
|
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Severe Combined Immunodeficiency Due To Artemis Deficiency
|
Severe Combined Immunodeficiency, Athabaskan Type
|
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SCIDA
|
Severe Combined Immunodeficiency, Athabascan-Type
|
|
Artemis Deficiency
|
Severe Combined Immunodeficiency Athabaskan Type
|
|
Severe Combined Immunodeficiency Autosomal Recessive T-Cell-Negative/B-Cell-Negative/Nk-Cell-Positive With Sensitivity To Ionizing Radiation
|
RSSCID
|
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Athabascan Scid
|
Immunodeficiency, Severe Combined, Athabascan Type
|
|
Severe Combined Immunodeficiency, Athabaskan-Type
|
|
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| Xeroderma Pigmentosum, Variant Type |
|
Xeroderma Pigmentosum
|
XPV
|
|
Xeroderma Pigmentosum Variant Type
|
Xeroderma Pigmentosum With Normal Dna Repair Rates
|
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Photosensitivity With Defective Dna Synthesis
|
Xp
|
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De Sanctis-Cacchione Syndrome
|
Desanctis-Cacchione Syndrome
|
|
Xeroderma Pigmentosa
|
Xerodermic Idiocy
|
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Xeroderma Pigmentosum Variant
|
Xp - [Xeroderma Pigmentosum]
|
|
Atrophoderma Pigmentosum
|
|
|
| Dyskeratosis Congenita |
|
Dyskeratosis Congenita Autosomal Dominant
|
Dc
|
|
Dkc
|
Zinsser-Engman-Cole Syndrome
|
|
Dyskeratosis Congenita, Autosomal Dominant
|
Autosomal Dominant Dyskeratosis Congenita
|
|
Dkca
|
Dyskeratosis Congenita Scoggins Type
|
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Zinsser-Cole-Engman Syndrome
|
X-Linked Dyskeratosis Congenita
|
|
Hoyeraal-Hreidarsson Syndrome
|
|
|
| Pancytopenia |
|
|
| Ataxia-Telangiectasia |
|
Ataxia Telangiectasia
|
Louis-Bar Syndrome
|
|
AT
|
At1
|
|
Ataxia-Telangiectasia Syndrome
|
Ataxia - Telangiectasia Variant
|
|
Boder-Sedgwick Syndrome
|
Louis Bar Syndrome
|
|
Cerebello-Oculocutaneous Telangiectasia
|
Immunodeficiency With Ataxia Telangiectasia
|
|
A-T
|
Ataxia Telangiectasia Syndrome
|
|
Atm
|
Telangiectasia, Cerebello-Oculocutaneous
|
|
Ataxia-Telangiectasia Variant
|
|
|
| Janus Kinase-3 Deficiency |
|
|
| Bare Lymphocyte Syndrome, Type Ii |
|
Mhc Class Ii Deficiency
|
Bare Lymphocyte Syndrome
|
|
Major Histocompatibility Complex Class Ii Deficiency
|
Bare Lymphocyte Syndrome 2
|
|
Bare Lymphocyte Syndrome Type 2
|
Severe Combined Immunodeficiency, Hla Class Ii-Negative
|
|
Bare Lymphocyte Syndrome, Type Ii, Complementation Group C
|
Bare Lymphocyte Syndrome, Type Ii, Complementation Group D
|
|
Bare Lymphocyte Syndrome Type Ii
|
Scid, Hla Class Ii-Negative
|
|
Bare Lymphocyte Syndrome, Type Ii, Complementation Group A
|
Bare Lymphocyte Syndrome, Type Ii, Complementation Group B
|
|
Scid Due To Absent Class Ii Hla Antigens
|
Hla Class 1 Deficiency
|
|
Scid, Hla Class 2-Negative
|
Bls Type Ii
|
|
Bare Lymphocyte Syndrome Type 2, Complementation Group A
|
Bare Lymphocyte Syndrome Type 2, Complementation Group E
|
|
Severe Combined Immunodeficiency
|
Bls, Type Ii
|
|
Bls
|
Bare Lymphocyte Syndrome, Type Ii, Complementation Group E
|
|
Blsii
|
Bls Type 1
|
|
Bls 2
|
Scid Due To Absence Of Class Ii Hla Antigens
|
|
Severe Combined Immunodeficiency Due To Absent Class Ii Human Leukocyte Antigens
|
Immunodeficiency By Defective Expression Of Mhc Class Ii
|
|
BLS2
|
Bare Lymphocyte Syndrome Type Ii Complementation Group A
|
|
Bare Lymphocyte Syndrome Type Ii Complementation Group B
|
Bare Lymphocyte Syndrome Type Ii Complementation Group C
|
|
Bare Lymphocyte Syndrome Type Ii Complementation Group D
|
Bare Lymphocyte Syndrome Type Ii Complementation Group E
|
|
Bls Ii
|
Hereditary Mhc Class Ii Deficiency
|
|
Hla Class Ii Deficient Combined Immunodeficiency
|
Mhc-Ii Deficiency
|
|
Scid Hla Class Ii-Negative
|
Severe Combined Immunodeficiency Hla Class Ii-Negative
|
|
Bl-2
|
Immunodeficiency By Defective Expression Of Hla Class 2
|
|
Hla Class 2-Negative Severe Combined Immunodeficiency
|
|
|
| Autosomal Recessive Cerebellar Ataxia |
|
|
| Immune Deficiency Disease |
|
Immunodeficiency
|
Primary Immunodeficiency
|
|
Primary Immunodeficiency Disease
|
Immunologic Deficiency Syndromes
|
|
Hypoimmunity
|
Immune Deficiency Disorder
|
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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
|
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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
|
|
|
| Medulloblastoma |
|
MDB
|
Cpnet
|
|
Localized Primitive Neuroectodermal Tumor
|
Classic Medulloblastoma
|
|
Medulloblastoma Predisposition Syndrome
|
Medulloblastoma, Somatic
|
|
Brain Medulloblastoma
|
Cns Pnet
|
|
Infratentorial Primitive Neuroectodermal Tumor
|
Neuroectodermal Tumors, Primitive
|
|
Medulloblastomas
|
Desmoplastic Medulloblastoma
|
|
Medulloblastoma, With Extensive Nodularity
|
Medulloblastoma Of Unspecified Site
|
|
Medullomyoblastoma Of Unspecified Site
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| 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
|
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer
|
|
Breast And/Or Ovarian Cancer
|
Breast And Ovarian Cancer Syndrome
|
|
Hboc Syndrome
|
Hereditary Breast And Ovarian Cancer
|
|
Brca1- Brca2-Associated Hboc
|
|
|
