| 疾病名称 |
别名 |
|
| Werner Syndrome |
|
Werner'S Syndrome
|
WRN
|
|
Adult Progeria
|
Ws
|
|
Adult Premature Ageing Syndrome
|
Adult Premature Aging Syndrome
|
|
Werners Syndrome
|
|
|
| Aicardi-Goutieres Syndrome |
|
Aicardi Goutieres Syndrome
|
Cree Encephalitis
|
|
Aicardi-Goutières Syndrome
|
Encephalopathy With Basal Ganglia Calcification
|
|
Ags
|
Encephalopathy With Intracranial Calcification And Chronic Lymphocytosis Of Cerebrospinal Fluid
|
|
Pseudotoxoplasmosis Syndrome
|
Encephalopathy, Familial Infantile, With Calcification Of Basal Ganglia And Chronic Cerebrospinal Fluid Lymphocytosis
|
|
Familial Infantile Encephalopathy With Intracranial Calcification And Chronic Cerebrospinal Fluid Lymphocytosis
|
Aicardi-Goutieres Syndrome 1
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
|
Familial Nonpolyposis Colon Cancer
|
Hnpcc
|
|
Coca 1
|
Hereditary Defective Mismatch Repair Syndrome
|
|
Hereditary Non-Polyposis Colon Cancer
|
Hereditary Non-Polyposis Colon Cancer Syndrome
|
|
Hereditary Non-Polyposis Colorectal Cancer
|
Hereditary Non-Polyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome
|
Hereditary Nonpolyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colorectal Neoplasm
|
Hnpcc - Hereditary Nonpolyposis Colon Cancer
|
|
Cancer Family Syndrome
|
Familial Nonpolyposis Colorectal Cancer
|
|
Colon Cancer, Familial Nonpolyposis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Cancer, Colorectal, Nonpolyposis, Hereditary
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
|
|
| Chilblain Lupus 1 |
|
Chilblain Lupus
|
CHBL1
|
|
Chilblain Lupus Erythematosus
|
Chle
|
|
Hutchinson Lupus
|
Chilblain Lupus, Type 1
|
|
|
| Mismatch Repair Cancer Syndrome |
|
Turcot Syndrome
|
Brain Tumor-Polyposis Syndrome 1
|
|
Btp1 Syndrome
|
Btps1
|
|
Childhood Cancer Syndrome
|
Cmmr-D Syndrome
|
|
Cmmrds
|
Constitutional Mismatch Repair Deficiency Syndrome
|
|
Mmr Deficiency
|
Cancer Syndrome, Mismatch Repair
|
|
Malignant Childhood Neoplasm
|
|
|
| Vasculopathy, Retinal, With Cerebral Leukoencephalopathy And Systemic Manifestations |
|
Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations
|
Crv
|
|
Rvcl
|
Rvcl-S
|
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy
|
Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
|
|
Retinal Vasculopathy With Cerebral Leukodystrophy
|
Retinal Vasculopathy And Cerebral Leukoencephalopathy
|
|
Hereditary Vascular Retinopathy
|
Hvr
|
|
RVCLS
|
Cerebroretinal Vasculopathy, Hereditary
|
|
Cerebroretinal Vasculopathy
|
Herns
|
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy, Formerly
|
Hereditary Cerebroretinal Vasculopathy
|
|
Hereditary Endotheliopathy, Retinopathy, Nephropathy, Stroke
|
Hereditary Systemic Angiopathy
|
|
Hsa
|
Retinal Vasculopathy With Cerebral Leukodystrophy With Systemic Manifestations
|
|
Adrvcl
|
Autosomal Dominant Retinal Vasculopathy With Cerebral Leukodystrophy
|
|
Hereditary Endotheliopathy With Retinopathy-Nephropathy-Stroke
|
Vascular Retinopathy With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
|
|
|
| Xeroderma Pigmentosum, Complementation Group G |
|
Xeroderma Pigmentosum, Group G
|
Xeroderma Pigmentosum Vii
|
|
Xp7
|
XPG
|
|
Xeroderma Pigmentosum Group G
|
Xp Group G
|
|
Xp, Group G
|
Xpgc
|
|
Xeroderma Pigmentosum, Group G/Cockayne Syndrome
|
Xeroderma Pigmentosum, Type 7
|
|
Xeroderma Pigmentosum Complementation Group G
|
XP-G
|
|
Xp-G/Cs
|
Xeroderma Pigmentosum Group G/Cockayne Syndrome
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Xeroderma Pigmentosum, Variant Type |
|
Xeroderma Pigmentosum
|
XPV
|
|
Xeroderma Pigmentosum Variant Type
|
Xeroderma Pigmentosum With Normal Dna Repair Rates
|
|
Photosensitivity With Defective Dna Synthesis
|
Xp
|
|
De Sanctis-Cacchione Syndrome
|
Desanctis-Cacchione Syndrome
|
|
Xeroderma Pigmentosa
|
Xerodermic Idiocy
|
|
Xeroderma Pigmentosum Variant
|
Xp - [Xeroderma Pigmentosum]
|
|
Atrophoderma Pigmentosum
|
|
|
| Nemaline Myopathy 3 |
|
Nemaline Myopathy 3, Autosomal Dominant Or Recessive
|
Congenital Myopathy With Excess Of Thin Filaments
|
|
NEM3
|
Myopathy, Actin, Congenital, With Cores
|
|
Myopathy, Actin, Congenital, With Excess Of Thin Myofilaments
|
Actin-Accumulation Myopathy
|
|
Actin Myopathy
|
Actin Accumulation Myopathy
|
|
Actin Filament Aggregate Myopathy
|
Nemaline Myopathy, Type 3
|
|
MPCETM
|
Acta1-Related Nemaline Myopathy
|
|
Actin Myopathy Congenital With Cores
|
Nemaline Myopathy 3 With Intranuclear Rods
|
|
Myopathy, Nemaline, Type 3
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Rothmund-Thomson Syndrome, Type 2 |
|
Rothmund-Thomson Syndrome
|
Rts
|
|
RTS2
|
Poikiloderma Of Rothmund-Thomson
|
|
Rothmund-Thomson Syndrome Type 2
|
Congenital Poikiloderma
|
|
Poikiloderma Congenitale
|
Poikiloderma Atrophicans And Cataract
|
|
Poikiloderma Congenitale Of Rothmund-Thomson
|
Poikiloderma Of Rothmund-Thomson Type 2
|
|
Rothmund-Thomson Syndrome 2
|
Erythrokeratodermia Variabilis
|
|
|
| Cutaneous Lupus Erythematosus |
|
Lupus Erythematosus, Cutaneous
|
Lupus Erythematosus Cutaneous
|
|
|
| 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
|
|
Microcephaly-Immunodeficiency-Lymphoreticuloma Syndrome
|
Microcephaly Immunodeficiency Lymphoreticuloma
|
|
Microcephaly With Normal Intelligence Immunodeficiency And Lymphoreticular Malignancies
|
Nonsyndromal Microcephaly Autosomal Recessive With Normal Intelligence
|
|
Seemanova Syndrome 2
|
Ataxia-Telangiectasia Variant 1
|
|
Seemanova Syndrome
|
At V1
|
|
Ataxia-Telangiectasia, Variant 1
|
Microcephaly-Immunodeficiency-Lymphoid Malignancy Syndrome
|
|
V-At
|
Ataxia Telangiectasia Variant V1
|
|
|
| Trichothiodystrophy |
|
Ttd
|
Amish Brittle Hair Syndrome
|
|
Bids Syndrome
|
Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome
|
|
Ibids
|
Pibids
|
|
Trichothiodystrophy Syndromes
|
|
|
| Cockayne Syndrome A |
|
Cockayne Syndrome Type 1
|
Cockayne Syndrome, Type A
|
|
Cockayne Syndrome Type I
|
CSA
|
|
Cockayne Syndrome Classic Form
|
Cockayne Syndrome Classical
|
|
Cockayne Syndrome Type A
|
Ckn1
|
|
|
| Seckel Syndrome |
|
Microcephalic Primordial Dwarfism
|
Bird-Headed Dwarfism
|
|
Harper'S Syndrome
|
Virchow-Seckel Dwarfism
|
|
Nanocephalic Dwarfism
|
Sckl
|
|
Seckel-Type Dwarfism
|
|
|
| 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
|
|
|
| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
|
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
|
|
|
