| 疾病名称 |
别名 |
|
| Fanconi Anemia, Complementation Group G |
|
Fanconi Anemia Complementation Group G
|
FANCG
|
|
|
| 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
|
|
|
| Fanconi Anemia, Complementation Group L |
|
Fanconi Anemia Complementation Group L
|
FANCL
|
|
|
| Pituitary Stalk Interruption Syndrome |
|
Ectopic Neurohypophysis
|
Psis
|
|
|
| Fanconi Anemia, Complementation Group E |
|
Fanconi Anemia Complementation Group E
|
FANCE
|
|
Face
|
Faces Syndrome
|
|
|
| Fanconi Anemia, Complementation Group F |
|
Fanconi Anemia Complementation Group F
|
FANCF
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Cancer Of The Pancreas
|
Pancreatic Carcinoma, Somatic
|
|
Pancreatic Cancer, Somatic
|
Ca Body Of Pancreas
|
|
Ca Head Of Pancreas
|
Ca Tail Of Pancreas
|
|
Malignant Neoplasm Of Body Of Pancreas
|
Malignant Neoplasm Of Head Of Pancreas
|
|
Malignant Neoplasm Of Tail Of Pancreas
|
Pancreas Neoplasm
|
|
Exocrine Cancer
|
Exocrine Pancreas Carcinoma
|
|
Hereditary Pancreatic Cancer
|
Hereditary Pancreatic Carcinoma
|
|
PNCA
|
Pancreatic Cancer, Susceptibility To
|
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
| Fanconi Anemia, Complementation Group D1 |
|
Fanconi Anemia Complementation Group D1
|
FANCD1
|
|
Fad1
|
Inherited Cancer-Predisposing Syndrome Due To Biallelic Brca2 Mutations
|
|
|
| Fanconi Anemia, Complementation Group B |
|
Fanconi Anemia Complementation Group B
|
FANCB
|
|
Facb
|
Fa2
|
|
Fanconi Pancytopenia Type 2
|
Fanconi Pancytopenia, Type 2
|
|
|
| Pancytopenia |
|
|
| Fanconi Anemia, Complementation Group U |
|
Fanconi Anemia Complementation Group U
|
FANCU
|
|
|
| Bloom Syndrome |
|
BLM
|
Bs
|
|
Bls
|
Bloom-Torre-Machacek Syndrome
|
|
Microcephaly, Growth Restriction, And Increased Sister Chromatid Exchange 1
|
Mgrisce1
|
|
Congenital Telangiectatic Erythema
|
Congenital Telangiectatic Erythema Syndrome
|
|
Growth Deficiency, Sun-Sensitive, Telangiectatic, Hypo And Hyperpigmented Skin, Predisposition To Malignancy And Chromosomal Instability
|
Bloom'S Syndrome
|
|
Bsyn
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Fanconi Anemia, Complementation Group T |
|
Fanconi Anemia Complementation Group T
|
FANCT
|
|
|
| Peliosis Hepatis |
|
Hepatic Peliosis
|
Telangiectasis Of Liver
|
|
Angiomatosis Of Liver
|
Ph - [Peliosis Hepatis]
|
|
Hepatic Angiomatosis
|
|
|
| Physical Disorder |
|
|
| Fanconi Anemia, Complementation Group D2 |
|
Fanconi Anemia Complementation Group D2
|
FANCD2
|
|
Fad2
|
Fa4
|
|
Fancd
|
Fanconi Pancytopenia Type 4
|
|
Fanconi Anemia, Complementation Group D
|
Fanconi Pancytopenia, Type 4
|
|
Facd
|
Fanconi Anemia Complementation Group D
|
|
|
| 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
|
|
|
| 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
|
|
|
| Squamous Cell Carcinoma, Head And Neck |
|
Squamous Cell Carcinoma Of The Head And Neck
|
HNSCC
|
|
Head And Neck Squamous Cell Carcinoma
|
Squamous Cell Carcinoma Of Lip
|
|
Squamous Cell Carcinoma, Head And Neck, Somatic
|
Carcinoma Of The Head And Neck
|
|
Squamous Cell Carcinomas Of Head And Neck
|
Scchn
|
|
Squamous Cell Carcinoma Of The Hypopharynx
|
Squamous Cell Carcinoma Of The Oropharynx
|
|
Squamous Cell Carcinoma Of Salivary Glands
|
Squamous Cell Carcinoma Of The Nasal Cavity And Paranasal Sinuses
|
|
Squamous Cell Carcinoma Of The Nasal Cavity And Sinuses
|
Squamous Cell Carcinoma Of The Oral Cavity
|
|
Squamous Cell Carcinoma Of The Lip
|
Carcinoma, Squamous Cell Of Head And Neck
|
|
Lip Squamous Cell Carcinoma
|
Carcinoma, Squamous Cell, Head And Neck
|
|
Salivary Gland Squamous Cell Carcinoma
|
Cancer Of Head And Neck
|
|
Squamous Cell Carcinoma Of Oropharynx Nos
|
|
|
| Shwachman-Diamond Syndrome 1 |
|
Shwachman-Diamond Syndrome
|
Shwachman Syndrome
|
|
Shwachman-Bodian-Diamond Syndrome
|
Sds
|
|
Pancreatic Insufficiency And Bone Marrow Dysfunction
|
Shwachman-Bodian Syndrome
|
|
SDS1
|
Lipomatosis Of Pancreas, Congenital
|
|
Congenital Lipomatosis Of Pancreas
|
Shwachman-Diamond Type Metaphyseal Dysplasia
|
|
Metaphyseal Chondrodysplasia, Shwachman Type
|
Shwachman-Diamond-Oski Syndrome
|
|
|
| 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
|
|
|
| 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
|
|
Zinsser-Cole-Engman Syndrome
|
X-Linked Dyskeratosis Congenita
|
|
Hoyeraal-Hreidarsson Syndrome
|
|
|
| Seckel Syndrome |
|
Microcephalic Primordial Dwarfism
|
Bird-Headed Dwarfism
|
|
Harper'S Syndrome
|
Virchow-Seckel Dwarfism
|
|
Nanocephalic Dwarfism
|
Sckl
|
|
Seckel-Type Dwarfism
|
|
|
| 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
|
|
|
| Diamond-Blackfan Anemia |
|
Congenital Pure Red Cell Aplasia
|
Aase Syndrome
|
|
Erythrogenesis Imperfecta
|
Anemia, Diamond-Blackfan
|
|
Congenital Hypoplastic Anemia
|
Aase-Smith Ii Syndrome
|
|
Bds
|
Blackfan-Diamond Anemia
|
|
Congenital Prca
|
Congenital Hypoplastic Anemia, Blackfan-Diamond Type
|
|
Dba
|
Blackfan - Diamond Syndrome
|
|
Chronic Constitutional Pure Red Cell Anaemia
|
Anemia Diamond Blackfan Type
|
|
Anemia Congenital Erythroid Hypoplastic
|
Aregenerative Anemia Chronic Congenital
|
|
Blackfan Diamond Syndrome
|
Red Cell Aplasia, Pure Hereditary
|
|
Aase-Smith Syndrome Ii
|
Bda
|
|
Blackfan Diamond Anemia
|
Blackfan-Diamond Disease
|
|
Blackfan-Diamond Syndrome
|
Chronic Congenital Agenerative Anemia
|
|
Congenital Erythroid Hypoplastic Anemia
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
|
|
Congenital Pure Red Cell Anemia
|
Hypoplastic Congenital Anemia
|
|
Inherited Erythroblastopenia
|
Pure Hereditary Red Cell Aplasia
|
|
Anemia, Hypoplastic, Congenital
|
Anemia Hypoplastic Congenital
|
|
Fanconi Anemia
|
Constitutional Aplastic Anemia
|
|
Diamond-Blackfan Anemia 1
|
Aase Smith Syndrome 2
|
|
Congenital Red Cell Aplasia
|
Red Cell Aplasia Of Infants
|
|
Pure Red Cell Aplasia Of Infants
|
Congenital Red Cell Aplastic Anaemia
|
|
Congenital Pure Red Cell Anaemia
|
Congenital Erythroid Hypoplasia
|
|
Pearson Marrow-Pancreas Syndrome
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
