| 疾病名称 |
别名 |
|
| Ehlers-Danlos Syndrome, Periodontal Type, 2 |
|
EDSPD2
|
Ehlers-Danlos Syndrome, Periodontal Type 2
|
|
Ehlers-Danlos Syndrome Periodontal Type 2
|
|
|
| Complement Component C1s Deficiency |
|
|
| Ehlers-Danlos Syndrome, Periodontal Type, 1 |
|
Ehlers-Danlos Syndrome, Type Viii
|
EDSPD1
|
|
Eds8
|
Eds Viii
|
|
Ehlers-Danlos Syndrome, Periodontitis Type
|
Ehlers-Danlos Syndrome, Periodontosis Type
|
|
Ehlers-Danlos Syndrome, Periodontal Type 1
|
Ehlers-Danlos Syndrome Periodontal Type 1
|
|
|
| Periodontal Ehlers-Danlos Syndrome |
|
Peds
|
Eds Viii
|
|
Ehlers-Danlos Syndrome Type 8
|
Ehlers-Danlos Syndrome, Periodontitis Type
|
|
Ehlers-Danlos Syndrome, Type Viii
|
Periodontal Eds
|
|
Eds Type Viii
|
Eds8
|
|
Ehlers-Danlos Syndrome, Periodontosis Type
|
|
|
| Immunodeficiency Due To A Classical Component Pathway Complement Deficiency |
|
Immunodeficiency Due To C1, C4, Or C2 Component Complement Deficiency
|
Immunodeficiency Due To An Early Component Of Complement Deficiency
|
|
|
| Hereditary Angioedema |
|
Hereditary Angioneurotic Edema
|
Hereditary Angioedema Type 1
|
|
Hane
|
Angioedema, Hereditary
|
|
Hae
|
Angioedemas, Hereditary
|
|
Deficiency Of C1 Esterase Inhibitor
|
C1 Esterase Inhibitor Deficiency
|
|
C1 Inhibitor Deficiency
|
Familial Angioneurotic Edema
|
|
Hereditary Bradykinine-Induced Angioedema
|
Hereditary Non Histamine-Induced Angioedema
|
|
Hae 1
|
Hae-I
|
|
Hereditary Angioneurotic Edema Type 1
|
Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor
|
|
Hereditary Angioedema Types I And Ii
|
Hereditary Angioneurotic Oedema
|
|
Familial Angioedema
|
Hae - [Hereditary Angioneurotic Oedema]
|
|
Bannister Disease, Hereditary
|
Quincke Disease Or Oedema
|
|
Hereditary Quincke Oedema
|
|
|
| Angioedema |
|
Angioneurotic Oedema
|
Quincke'S Edema
|
|
Angioneurotic Edema
|
Giant Urticaria
|
|
|
| Gingival Recession |
|
Localized Gingival Recession
|
Gingival Recession, Localized
|
|
Minimal Gingival Recession
|
Moderate Gingival Recession
|
|
Severe Gingival Recession
|
Gingival Recession, Minimal
|
|
Gingival Recession, Severe
|
Atrophy Of Gums
|
|
Gum Atrophy
|
Gingival Atrophy
|
|
|
| Urticaria |
|
Nettle Rash
|
Hives
|
|
Wheal
|
Urticaria Nos
|
|
|
| Capillary Leak Syndrome |
|
Systemic Capillary Leak Syndrome
|
Clarkson Disease
|
|
Capillary Leak Syndrome With Monoclonal Gammopathy
|
Scls
|
|
Periodic Systemic Capillary Leak Syndrome
|
Capillary Hyperpermeability Syndrome
|
|
Idiopathic Capillary Leak Syndrome
|
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Glomerulonephritis |
|
|
| Spondylocostal Dysostosis 2, Autosomal Recessive |
|
SCDO2
|
Spondylocostal Dysostosis, Autosomal Recessive 2
|
|
Spondylocostal Dysostosis 2
|
Autosomal Recessive Spondylocostal Dysostosis 2
|
|
Doid:0112362
|
Dysostosis, Spondylocostal, Autosomal Recessive, Type 2
|
|
|
| Acquired Angioedema |
|
Acquired C1 Inhibitor Deficiency
|
Angioedema, Acquired
|
|
Aae
|
Acquired Angioneurotic Edema
|
|
Acquired Bradykinine-Induced Angioedema
|
Acquired Non Histamine-Induced Angioedema
|
|
Acquired Angioneurotic Oedema
|
Aae - [Acquired Angioneurotic Oedema]
|
|
|
| Lupus Erythematosus |
|
Lupus
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus, Systemic
|
|
Subacute Cutaneous Lupus
|
Le - [Lupus Erythematosus]
|
|
|
| Laryngeal Small Cell Carcinoma |
|
Small Cell Carcinoma Of Larynx
|
|
|
| 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]
|
|
|
| Vasculitis |
|
Angiitis
|
Autoimmune Vasculitis
|
|
Systemic Vasculitis
|
Vasculitis, Autoimmune
|
|
|
| Hemolytic-Uremic Syndrome |
|
Hemolytic Uremic Syndrome
|
Haemolytic-Uraemic Syndrome
|
|
Hus
|
Acute Renal Failure, Thrombocytopenia, And Microangiopathic Hemolytic Anemia Associated With Distorted Erythrocytes
|
|
Typical Haemolytic Uraemic Syndrome
|
Gasser Syndrome
|
|
Hus - [Haemolytic Uraemic Syndrome]
|
|
|
| C1 Inhibitor Deficiency |
|
Quincke Edema
|
Angioedemas, Hereditary
|
|
Angioedema
|
|
|
| Angioedema, Hereditary, 1 |
|
Hereditary Angioedema Type I
|
Hereditary Angioneurotic Edema
|
|
Hane
|
C1 Esterase Inhibitor Deficiency
|
|
Angioedema, Hereditary, 1 And 2
|
HAE1
|
|
Angioneurotic Edema, Hereditary
|
Angioedema, Hereditary, Type I
|
|
Hereditary Angioedema Type 2
|
Hae 2
|
|
Hae-Ii
|
Hereditary Angioneurotic Edema Type 2
|
|
Angioedema, Hereditary
|
HAE
|
|
Angioedema, Hereditary, Types I And Ii
|
Hereditary Angioedema, Type Ii
|
|
Angioedema, Hereditary, Type 1
|
Angioedemas, Hereditary
|
|
Hereditary C1 Esterase Inhibitor Deficiency - Dysfunctional Factor
|
Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor
|
|
Hereditary Angioedema Types I And Ii
|
|
|
| Complement Component 3 Deficiency |
|
|
| Angioedema, Hereditary, 3 |
|
Angioedema, Hereditary, Type Iii
|
Hereditary Angioedema Type Iii
|
|
Hereditary Angioedema Type 3
|
HAE3
|
|
Estrogen-Related Hae
|
Estrogen-Sensitive Hae
|
|
Angioneurotic Edema, Hereditary, With Normal C1 Inhibitor Concentration And Function
|
Hae With Normal C1 Inhibitor Concentration And Function
|
|
Hereditary Angioedema With Normal C1 Inhibitor Activity
|
F12-Related Hereditary Angioedema With Normal C1inh
|
|
F12-Related Hae With Normal C1 Inhibitor
|
Hae 3
|
|
Hae-Iii
|
Hereditary Angioneurotic Edema Type 3
|
|
Inherited Estrogen-Associated Angioedema
|
Inherited Estrogen-Associated Angioneurotic Edema
|
|
Inherited Estrogen-Dependent Angioedema
|
Inherited Estrogen-Dependent Angioneurotic Edema
|
|
Angioneurotic Edema Hereditary With Normal C1 Inhibitor Concentration And Function
|
Hereditary Angioedema With Normal C1 Esterase Inhibitor Activity
|
|
|
| Complement Deficiency |
|
Complement Deficiency Disease
|
Hereditary Complement Deficiency Diseases
|
|
|
| Vulvar Angiokeratoma |
|
Fordyce Angiokeratoma Of Vulva
|
Angiokeratoma Of Vulva
|
|
|
| Louse-Borne Relapsing Fever |
|
Relapsing Fever, Louse-Borne
|
Relapsing Fever Due To Borrelia Recurrentis
|
|
|
| 3mc Syndrome |
|
Craniofacial-Ulnar-Renal Syndrome
|
Malpuech Facial Clefting Syndrome
|
|
Oculopalatoskeletal Syndrome
|
Carnevale Syndrome
|
|
Michels Syndrome
|
Malpuech-Michels-Mingarelli-Carnevale Syndrome
|
|
Carnevale-Krajewska-Fischetto Syndrome
|
Craniosynostosis With Lid Anomalies
|
|
Malpuech Syndrome
|
Mingarelli Syndrome
|
|
Oculo-Skeletal-Abdominal Syndrome
|
Osa Syndrome
|
|
Ptosis Of Eyelids With Diastasis Recti And Hip Dysplasia
|
Ptosis-Strabismus-Rectus Abdominis Diastasis
|
|
|
| Transposition Of The Great Arteries, Dextro-Looped |
|
Transposition Of The Great Arteries
|
DTGA1
|
|
Dextro-Looped Transposition Of The Great Arteries
|
DTGA
|
|
Congenitally Uncorrected Transposition Of The Great Arteries
|
Congenitally Uncorrected Transposition Of The Great Vessels
|
|
D-Tga
|
Isolated Ventriculoarterial Discordance
|
|
Ventriculoarterial Discordance With Atrioventricular Concordance
|
Dextro-Transposition Of The Great Arteries
|
|
Transposition Of The Great Vessels
|
Great Vessels Transposition
|
|
Transposition Of The Great Arteries, Dextro-Looped 1
|
Arteries, Great, Transposition, Dextro-Looped
|
|
Ventriculoarterial Discordance, Isolated
|
D-Transposition Of The Great Arteries
|
|
Complete Transposition
|
Tga
|
|
Tgv
|
Transposition Of Great Vessels
|
|
Transposition Of The Great Arteries Dextro-Looped 1
|
Dextro-Looped Transposition Of The Great Arteries 1
|
|
Discordant Ventriculoarterial Connection
|
Complete Transposition Of Great Vessels
|
|
Great Vessels Complete Transposition
|
Total Great Vessel Transposition
|
|
Transposition Of Great Arteries
|
Complete Tga - [Transposition Of The Great Arteries]
|
|
Tga - [Transposition Of Great Arteries]
|
Tgv - [Transposition Of Great Vessels]
|
|
Transposition Of Great Vessels Nos
|
Transposed Vessels Nos
|
|
|
| Macroglossia |
|
Congenital Macroglossia
|
Enlarged Tongue
|
|
Giant Tongue
|
Acquired Macroglossia Nos
|
|
Congenital Hypertrophy Of Tongue
|
|
|
| Complement Component 5 Deficiency |
|
|
| 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
|
|
|
| Meningococcal Meningitis |
|
Meningitis, Meningococcal
|
Meningitis Meningococcal
|
|
Epidemic Meningitis
|
Meningitis Due To Neisseria Meningitidis
|
|
Meningococcal Meninges Infection
|
Meningococcal Meningeal Infection
|
|
Meningococcal Cerebrospinal Inflammation
|
Chronic Meningococcal Arachnoiditis
|
|
Meningococcal Arachnoiditis
|
Diplococcal Spinal Meningitis
|
|
Diplococcal Meningitis
|
Meningococcal Cerebrospinal Fever
|
|
Meningococcal Cerebrospinal Infection
|
Meningococcal Spinal Meningitis
|
|
|
| Hemolytic Uremic Syndrome, Atypical 1 |
|
Atypical Hemolytic-Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
|
|
Atypical Hemolytic Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To
|
|
Ahus
|
AHUS1
|
|
Hemolytic-Uremic Syndrome
|
Ahus 1
|
|
Ahus, Susceptibility To, 1
|
Hemolytic Uremic Syndrome, Atypical
|
|
Non-Shiga-Like Toxin-Associated Hus
|
Non-Stx-Hus
|
|
Nonenteropathic Hus
|
Atypical Hus
|
|
Shiga Toxin-Associated Hemolytic Uremic Syndrome
|
D+ Hus
|
|
Ehec-Hus
|
Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli
|
|
Hemolytic Uremic Syndrome With Diarrhea
|
Stec-Hus
|
|
Shiga-Like Toxin-Associated Hus
|
Stx-Hus
|
|
Typical Hus
|
Typical Hemolytic Uremic Syndrome
|
|
Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies
|
Atypical Hus With Anti-Factor H Antibodies
|
|
Ahus With Anti-Factor H Antibodies
|
Ahus With Neutralizing Autoantibodies Against Factor H
|
|
Hemolytic Uremic Syndrome Atypical 1
|
Atypical Hemolytic Uremic Syndrome With H Factor Anomaly
|
|
D Hus
|
Hemolytic-Uremic Syndrome Without Diarrhea
|
|
Hemolytic-Uremic Syndrome, Atypical, Type 1
|
Hemolytic Uremic Syndrome, Typical
|
|
|
| Membranoproliferative Glomerulonephritis |
|
Mesangiocapillary Glomerulonephritis
|
Dense Deposit Disease
|
|
Membranoproliferative Glomerulonephritis Type 2
|
Primary Membranoproliferative Glomerulonephritis
|
|
Mesangiocapillary Glomerulonephritis, Type Ii
|
Glomerulonephritis, Membranoproliferative
|
|
Chronic Glomerulonephritis, Lobular
|
Lobular Glomerulonephritis
|
|
Ddd
|
Glomerulonephritis Membranoproliferative Type 2
|
|
Mpgn 2
|
Membranoproliferative Glomerulonephritis Type Ii
|
|
Mesangiocapillary Glomerulonephritis Type 2
|
Mpgn
|
|
Primary Mpgn
|
Glomerulonephritis Membranoproliferative
|
|
Membranoproliferative Glomerulonephritis, Type Ii
|
|
|
| Macular Degeneration, Age-Related, 1 |
|
Macular Degeneration
|
Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related
|
Age Related Macular Degeneration
|
|
Age Related Macular Degeneration 1
|
ARMD1
|
|
Senile Macular Degeneration
|
Maculopathy, Age-Related, 1
|
|
Macular Degeneration, Age-Related, Reduced Risk Of
|
Age Related Maculopathy 1
|
|
Age Related Maculopathies
|
Age Related Maculopathy
|
|
Senile Macular Retinal Degeneration
|
Macular Degeneration Of Retina
|
|
Age-Related Maculopathy
|
Amd
|
|
Armd
|
Age-Related Maculopathy, Susceptibility To
|
|
Maculopathy Age-Related
|
Macular Degeneration, Age-Related, 1, Susceptibility To
|
|
Maculopathy, Age-Related
|
Macular Degeneration, Age-Related, Type 1
|
|
Macular Degeneration, Age-Related, 2
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
