| Diseases |
Alias |
|
| Complement Factor I Deficiency |
|
Complement Component 3 Inactivator Deficiency
|
C3 Inactivator Deficiency
|
|
Hereditary Factor I Deficiency Disease
|
C3 Glomerulopathy 2
|
|
CFID
|
C3g2
|
|
Immunodeficiency With Factor I Anomaly
|
Complete Factor I Deficiency
|
|
CFI DEFICIENCY
|
Deficiency, Complement Factor I
|
|
Complement Factor I Deficiency
|
Deficiency Of Factor 1
|
|
Hereditary Fibrinogen Deficiency
|
Deficiency Of Fibrinogen
|
|
Congenital Fibrinogenopenia
|
|
|
| Macular Degeneration, Age-Related, 13 |
|
Age Related Macular Degeneration 13
|
ARMD13
|
|
Macular Degeneration, Age-Related, 13, Susceptibility To
|
Macular Degeneration, Age-Related, Type 13
|
|
|
| Hemolytic Uremic Syndrome, Atypical 3 |
|
AHUS3
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 3
|
|
Atypical Hemolytic-Uremic Syndrome With I Factor Anomaly
|
Ahus 3
|
|
Ahus, Susceptibility To, 3
|
Hemolytic Uremic Syndrome Atypical 3
|
|
Atypical Hemolytic Uremic Syndrome With I Factor Anomaly
|
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| Familial Drusen |
|
Malattia Leventinese
|
Doyne Honeycomb Retinal Dystrophy
|
|
Dhrd
|
Dominant Drusen
|
|
Dominant Radial Drusen
|
|
|
| Atypical Hemolytic Uremic Syndrome With Complement Gene Abnormality |
|
Atypical Hus With Complement Gene Abnormality
|
Ahus With Complement Gene Abnormality
|
|
|
| Hellp Syndrome |
|
Hemolysis, Elevated Liver Enzymes, Lowered Platelets
|
Hemolysis, Elevated Liver Enzymes, Low Platelets In Pregnancy
|
|
Hemolysis-Elevated Liver Enzymes-Low Platelets Syndrome
|
Hellp - [Syndrome Of Haemolysis, Elevated Liver Enzymes And Low Platelet]
|
|
Haemolysis-Elevated Liver Enzymes-Low Platelet Count Syndrome
|
|
|
| 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]
|
|
|
| De Novo Thrombotic Microangiopathy After Kidney Transplantation |
|
|
| Glomerulonephritis |
|
|
| 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
|
|
|
| D-Minus Hemolytic Uremic Syndrome |
|
Atypical Hus
|
Atypical Hemolytic Uremic Syndrome
|
|
Hus, Atypical
|
Ahus
|
|
|
| Meningitis |
|
Streptococcal Meningitis
|
Acute Streptococcal Meningitis
|
|
Staphylococcal Meningitis
|
Adenoviral Meningitis
|
|
Influenza Meningitis
|
Influenzal Meningitis
|
|
Meningitis Due To H. Influenzae
|
Cryptococcal Meningitis
|
|
Fungal Meningitis Due To Cryptococcus Neoformans
|
Cryptococcosis Meningitis
|
|
Cryptococcus Meningitis
|
Cryptococcal Meningoencephalitis
|
|
Meningitis Due To Cryptococcus
|
Mumps Virus Meningitis
|
|
Mumps Meningitis
|
|
|
| Thrombotic Thrombocytopenic Purpura |
|
Purpura, Thrombotic Thrombocytopenic
|
Ttp
|
|
Thrombotic Thrombocytopenic Purpura, Acquired
|
Idiopathic Thrombotic Thrombocytopenic Purpura
|
|
Moschcowitz Disease
|
Moschcowitz'S Syndrome
|
|
Moschowitz Syndrome
|
Chronic Relapsing Thrombotic Thrombocytopenic Purpura
|
|
Familial Thrombotic Thrombocytopenia Purpura
|
Moschkowitz Disease
|
|
Purpura Thrombotic Thrombocytopenic
|
Familial Thrombotic Thrombocytopenic Purpura
|
|
Microangiopathic Hemolytic Anemia
|
Congenital Thrombotic Thrombocytopenic Purpura
|
|
Autoimmune Thrombotic Thrombocytopenic Purpura
|
Ttp - [Thrombotic Thrombocytopenic Purpura]
|
|
Moschcowitz Syndrome
|
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| Hemoglobinuria |
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| End Stage Renal Disease |
|
End Stage Renal Failure
|
End-Stage Kidney Disease
|
|
Kidney Failure, Chronic
|
Chronic Kidney Disease Stage 5
|
|
|
| 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
|
|
|
| Complement Deficiency |
|
Complement Deficiency Disease
|
Hereditary Complement Deficiency Diseases
|
|
|
| Lyme Disease |
|
Lyme Borreliosis
|
Lyme Neuroborreliosis
|
|
Borreliosis
|
Borrelia Burgdorferi Infection
|
|
Neuroborreliosis
|
Bannwarth Syndrome
|
|
Bannworth'S Syndrome
|
Neurological Lyme Disease
|
|
B. Burgdorferi Infection
|
Borreliosis, Lyme
|
|
Infection By Borrelia Burgdorferi
|
Infection Due To Borrelia Burgdorferi Sensu Lato
|
|
Lym
|
Borrelia Infections
|
|
|
| Laron Syndrome |
|
Growth Hormone Insensitivity Syndrome
|
Growth Hormone Receptor Deficiency
|
|
Laron Dwarfism
|
Pituitary Dwarfism Ii
|
|
Laron-Type Isolated Somatotropin Defect
|
Primary Growth Hormone Resistance
|
|
Laron-Type Dwarfism
|
Laron Type Pituitary Dwarfism I
|
|
Primary Growth Hormone Insensitivity
|
Primary Gh Resistance
|
|
Gh-R Deficiency
|
Growth Hormone Receptor Defect
|
|
Laron-Type Pituitary Dwarfism
|
Laron-Type Short Stature
|
|
Severe Gh Insensitivity
|
Ghis
|
|
Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway
|
Complete Growth Hormone Insensitivity
|
|
Gh Receptor Deficiency
|
Primary Gh Insensitivity
|
|
Short Stature Due To Growth Hormone Resistance
|
LARS
|
|
|
| Acute Hemorrhagic Leukoencephalitis |
|
Ahl
|
Acute Haemorrhagic Leucoencephalitis Of Weston Hurst
|
|
Leukoencephalitis, Acute Hemorrhagic
|
Acute Hemorrhagic Encephalomyelitis
|
|
Acute Necrotizing Hemorrhagic Leukoencephalitis
|
Weston-Hurst Syndrome
|
|
Ahle
|
Acute Haemorrhagic Leucoencephalitis
|
|
Hurst Disease
|
Acute Haemorrhagic Leukoencephalitis, Postimmunization Or Postvaccinal
|
|
Postimmunization Or Postvaccinal Leukoencephalopathy
|
|
|
| Degeneration Of Macula And Posterior Pole |
|
Degeneration Of Macula And Posterior Pole Of Retina
|
Degeneration Of Macula Or Posterior Pole
|
|
Macular Degeneration Nos
|
Degenerative Disorder Of Macula
|
|
Drusen Macular Degeneration
|
Posterior Pole Macular Degeneration Of Eye
|
|
Macular Eye Degeneration
|
Macular Degeneration Of Retina, Unspecified
|
|
Pseudohole Degeneration Of Macula Of Retina
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Basal Laminar Drusen |
|
Drusen Of Bruch Membrane
|
Drusen, Cuticular
|
|
Drusen, Early Adult-Onset, Grouped
|
Cuticular Drusen
|
|
Early Adult-Onset Grouped Drusen
|
BLD
|
|
Drusen Cuticular
|
Drusen Early Adult-Onset Grouped
|
|
|
| Complement Component 3 Deficiency |
|
|
| 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
|
|
|
| Retinal Drusen |
|
|
| 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]
|
|
|
| Methylmalonic Aciduria And Homocystinuria, Cblc Type |
|
MAHCC
|
Vitamin B12 Metabolic Defect With Combined Deficiency Of Methylmalonyl-Coa Mutase And Homocysteine:Methyltetrahydrofolate Methyltransferase
|
|
Methylmalonic Aciduria And Homocystinuria, Cblc Type, Digenic
|
Methylmalonic Aciduria And Homocystinuria Type Cblc
|
|
Cobalamin C Disease
|
Methylmalonic Acidemia With Homocystinuria Cblc
|
|
Methylmalonic Acidemia And Homocystinuria, Cblc Type
|
Methylmalonic Aciduria And Homocystinuria, Vitamin B12-Responsive
|
|
Cobalamin C Deficiency
|
Methylmalonic Acidemia With Homocystinuria, Type Cblc
|
|
Cblc Defect
|
Cobalamin C Defect
|
|
Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cblc
|
Methylmalonic Aciduria With Homocystinuria, Type Cblc
|
|
Methylmalonic Acidemia And Homocystinuria Cblc Type
|
Methylmalonic Aciduria And Homocystinuria Vitamin B12-Responsive
|
|
Aciduria, Methylmalonic, And Homocystinuria, Cblc Type
|
Methylmalonic Acidemia With Homocystinuria
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Prader-Willi Syndrome |
|
Prader-Labhart-Willi Syndrome
|
PWS
|
|
Willi-Prader Syndrome
|
Prader-Willi Syndrome Due To Translocation
|
|
Prader-Willi Syndrome Due To Imprinting Mutation
|
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15
|
|
Prader Willi Syndrome
|
Upd(15)Mat
|
|
|
| Alcohol Dependence |
|
Alcoholism
|
Alcohol Dependence, Susceptibility To
|
|
Alcohol Dependence, Protection Against
|
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against
|
|
Alcoholism, Susceptibility To
|
Alcoholic Intoxication, Chronic
|
|
Pharyngeal Neoplasms
|
Chronic Alcoholism
|
|
Dipsomania
|
Alcohol Addiction
|
|
Ethanol Dependence
|
Chronic Ethanolism
|
|
Chronic Alcoholic Disease Nos
|
Alcoholic Disease Nos
|
|
Alcoholic
|
|
|
