| 疾病名称 |
别名 |
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Hyperchlorhidrosis, Isolated |
|
Isolated Hyperchlorhidrosis
|
HYCHL
|
|
Carbonic Anhydrase Xii Deficiency
|
|
|
| Bronchiectasis 3 |
|
|
| Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease |
|
Polycystic Kidney Disease 1
|
PKD1
|
|
Adpkd
|
Polycystic Kidney Disease, Adult, Type I
|
|
Apkd1
|
Potter Type Iii Polycystic Kidney Disease
|
|
Polycystic Kidney Disease, Adult
|
Potter Type Iii Polycystic Kidney Disease, Formerly
|
|
Polycystic Kidney Disease, Type 1
|
Adpkd1
|
|
Adult Polycystic Kidney Disease Type 1
|
Autosomal Dominant Polycystic Kidney Disease 1
|
|
Pkd-1
|
Polycystic Kidney Disease Adult
|
|
Polycystic Kidney Disease Type I
|
Polycystic Kidneys
|
|
Polycystic Kidney Disease, Adult Type I
|
Polycystic Kidney Type 1 Autosomal Dominant Disease
|
|
Kidney Disease, Polycystic, Type 1
|
Polycystic Kidney, Autosomal Dominant
|
|
Polycystic Kidney, Type 1 Autosomal Dominant Disease
|
Polycystic Kidney Diseases
|
|
|
| Bacterial Infectious Disease |
|
Bacterial Infections
|
Bacterial Infection Nos
|
|
Disease Caused By Bacteria
|
Bacterial Disease Or Disorder
|
|
|
| Alpha-1-Antitrypsin Deficiency |
|
Alpha 1-Antitrypsin Deficiency
|
Alpha-1 Antitrypsin Deficiency
|
|
Aat Deficiency
|
Aatd
|
|
A1ATD
|
Emphysema Due To Aat Deficiency
|
|
A1at Deficiency
|
Hemorrhagic Diathesis Due To Antithrombin Pittsburgh
|
|
Emphysema-Cirrhosis, Due To Aat Deficiency
|
Alpha-1 Antiprotease Deficiency
|
|
Alpha 1 Antitrypsin Deficiency
|
Aat
|
|
Alpha-1 Protease Inhibitor Deficiency
|
Alpha-1 Related Emphysema
|
|
Genetic Emphysema
|
Hereditary Pulmonary Emphysema
|
|
Inherited Emphysema
|
Alpha-1-Proteinase Inhibitor Deficiency
|
|
Alpha1-Antitrypsin Deficiency
|
Alpha-1-Antitrypsin Deficiency, Autosomal Recessive
|
|
Emphysema, Hereditary Pulmonary
|
Aatd - [Alpha-1-Antitrypsin] Deficiency
|
|
|
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Autosomal Recessive Polycystic Kidney Disease
|
Arpkd
|
|
Polycystic Kidney Disease, Autosomal Recessive
|
Polycystic Kidney And Hepatic Disease 1
|
|
Pkhd1
|
PKD4
|
|
Polycystic Kidney Disease 4 With Or Without Hepatic Disease
|
Polycystic Kidney Disease, Infantile, Type I
|
|
Polycystic Kidney Disease, Infantile Type
|
Polycystic Kidney, Autosomal Recessive
|
|
Pkd3, Formerly
|
Polycystic Kidney Disease 4, With Or Without Hepatic Disease
|
|
Arpkd/Chf
|
Ar-Pkd
|
|
Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease
|
Infantile Polycystic Kidney Disease Type I
|
|
Pkd3
|
Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease
|
|
Polycystic Kidney Disease 3, Autosomal Dominant
|
|
|
| Young Syndrome |
|
Sinusitis-Infertility Syndrome
|
Azoospermia-Sinopulmonary Infections Syndrome
|
|
Azoospermia, Obstructive, And Chronic Sinopulmonary Infections
|
Barry-Perkins-Young Syndrome
|
|
Azoospermia Obstructive And Chronic Sinopulmonary Infections
|
Barry Perkins Young Syndrome
|
|
Azoospermia - Sinopulmonary Infections
|
|
|
| Spermatogenic Failure 10 |
|
SPGF10
|
Spermatogenic Failure With Defective Sperm Annulus
|
|
Spermatogenic Failure, Type 10
|
|
|
| Pulmonary Disease, Chronic Obstructive |
|
Chronic Obstructive Pulmonary Disease
|
COPD
|
|
Pulmonary Disease, Chronic Obstructive, Severe Early-Onset
|
Chronic Obstructive Lung Disease
|
|
Chronic Obstructive Airway Disease
|
Pulmonary Disease, Chronic Obstructive, Susceptibility To
|
|
Cold
|
Severe Early-Onset Chronic Obstructive Pulmonary Disease
|
|
Pulmonary Disease Chronic Obstructive
|
Pulmonary Disease, Obstructive, Chronic, Susceptibility To
|
|
Chronic Obstructive Pulmonary Disease Of Horses
|
Common Cold
|
|
Upper Respiratory Infections
|
Copd - [Chronic Obstructive Pulmonary Disease]
|
|
Coad - [Chronic Obstructive Airways Disease]
|
Cold - [Chronic Obstructive Lung Disease]
|
|
Chronic Airway Disease Nos
|
Chronic Airways Limitation, Unspecified
|
|
Chronic Obstructed Airway, Unspecified
|
Chronic Obstructive Airway Disease, Unspecified
|
|
Chronic Obstructive Airway, Unspecified
|
Obstructive Lung Disease Nos
|
|
Chronic Obstructive Lung Disease Nos
|
Chronic Obstructive Lung Nos
|
|
Obstructive Pulmonary Disease Nos
|
Exacerbation Copd Nos
|
|
Acute Exacerbation Copd
|
|
|
| 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
|
|
|
| Primary Biliary Cholangitis |
|
Primary Biliary Cirrhosis
|
Biliary Liver Cirrhosis
|
|
Chronic Nonsuppurative Destructive Cholangitis
|
Familial Primary Biliary Cirrhosis
|
|
Pbc
|
Hanot Syndrome
|
|
Cholestatic Cirrhosis
|
Biliary Cirrhosis Primary
|
|
Liver Cirrhosis, Biliary
|
Hanot'S Cirrhosis
|
|
Biliary Cirrhosis
|
Pericholangiolic Biliary Cirrhosis
|
|
Tannhauser-Magendantz Syndrome
|
Hanot-Rossle Syndrome
|
|
Hypertrophic Cirrhosis
|
Todd Cirrhosis
|
|
Hanot Cirrhosis
|
Charcot Cirrhosis
|
|
Mahon-Tannhauser Syndrome
|
Toxic Cirrhosis
|
|
Hypertrophic Biliary Cirrhosis
|
Monolobular Cirrhosis
|
|
Unilobar Cirrhosis
|
Xanthomatous Biliary Cirrhosis
|
|
|
| Hyperuricemia, Pulmonary Hypertension, Renal Failure, And Alkalosis Syndrome |
|
Hupra Syndrome
|
Alkalosis
|
|
HUPRAS
|
Hyperuricemia, Pulmonary Hypertension, Renal Failure, And Alkalosis
|
|
Hyperuricemia, Pulmonary Hypertension, Renal Failure, Alkalosis Syndrome
|
Hyperuricemia-Pulmonary Hypertension-Renal Failure-Alkalosis Syndrome
|
|
Alkalosis Nos
|
|
|
| Acute Necrotizing Pancreatitis |
|
Acute Pancreatitis
|
Pancreatitis, Acute Necrotizing
|
|
Pancreatitis Necrotizing
|
Necrotizing Pancreatitis
|
|
Pancreatitis
|
Pancreatitis Nos
|
|
Acute Pancreas Inflammation
|
|
|
| Pseudoxanthoma Elasticum |
|
PXE
|
Gronblad-Strandberg Syndrome
|
|
Pseudoxanthoma Elasticum, Modifier Of Severity Of
|
Gronblad-Strandberg-Touraine Syndrome
|
|
Gronblad Strandberg Syndrome
|
Groenblad-Strandberg Syndrome
|
|
Nevus Elasticus
|
Pxe - [Pseudoxanthoma Elasticum]
|
|
|
| Cystic Kidney Disease |
|
Renal Cyst
|
Simple Renal Cyst
|
|
Kidney Cysts
|
Kidney Diseases, Cystic
|
|
Renal Cysts
|
Kidney Cyst
|
|
Cystic Kidney
|
Congenital Cystic Kidney Disease
|
|
Cystic Kidney Diseases
|
Bosniak 1 Cyst
|
|
|
| Vas Deferens, Congenital Bilateral Aplasia Of |
|
Congenital Bilateral Absence Of Vas Deferens
|
CBAVD
|
|
Cavd
|
Congenital Bilateral Aplasia Of Vas Deferens
|
|
Congenital Bilateral Absence Of The Vas Deferens
|
Congenital Bilateral Agenesis Of Vas Deferens
|
|
Absence Of Vas Deferens
|
Absent Vasa
|
|
Congenital Absence Of Vas Deferens
|
Congenital Aplasia Of Vas Deferens
|
|
Absent Vas Deferens
|
Vas Deferens, Congenital Bilateral Absence
|
|
|
| Chylomicron Retention Disease |
|
CMRD
|
Anderson Disease
|
|
Lipid Transport Defect Of Intestine
|
Hypobetalipoproteinemia With Accumulation Of Apolipoprotein B-Like Protein In Intestinal Cells
|
|
Andd
|
Anderson Syndrome
|
|
Crd
|
Andersons Disease
|
|
Malabsorption Syndrome
|
|
|
| Protein-Energy Malnutrition |
|
PEM
|
Protein Energy Malnutrition
|
|
|
| Bronchitis |
|
Chronic Bronchitis
|
Acute Bronchitis
|
|
Bronchitis, Chronic
|
Acute Bronchitis And Bronchiolitis
|
|
Chest Cold
|
Chest Infection
|
|
Ci - Chest Infection
|
Recurrent Wheezy Bronchitis
|
|
Bronchitis Chronic
|
Lower Respiratory Tract Infection
|
|
Acute Lower Respiratory Tract Infection
|
Chronic Bronchitis Nos
|
|
Senile Bronchitis
|
Bronchitis Nos In Those Under L5 Years Of Age
|
|
Bronchitis Nos
|
|
|
| Hemochromatosis, Type 1 |
|
Hemochromatosis
|
Hemochromatosis Type 1
|
|
Hereditary Hemochromatosis
|
Hh
|
|
HFE1
|
Hfe Hemochromatosis, Modifier Of
|
|
Symptomatic Form Of Classic Hemochromatosis
|
Symptomatic Form Of Hemochromatosis Type 1
|
|
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis
|
Haemochromatosis
|
|
Iron Storage Disorder
|
Bronze Diabetes
|
|
Hlah
|
Hfe
|
|
Hemochromatosis, Hereditary
|
Diabetes Bronze
|
|
Classic Hemochromatosis
|
Hfe-Associated Hereditary Hemochromatosis
|
|
Hemochromatosis Classic
|
Bronzed Cirrhosis
|
|
Familial Hemochromatosis
|
Genetic Hemochromatosis
|
|
Hc
|
Hereditary Haemochromatosis
|
|
Pigmentary Cirrhosis
|
Primary Hemochromatosis
|
|
Troisier-Hanot-Chauffard Syndrome
|
Von Recklenhausen-Applebaum Disease
|
|
Hemochromatosis 1
|
Primary Hereditary Hemochromatosis
|
|
Bronze Cirrhosis
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Autosomal Dominant Polycystic Kidney Disease |
|
Polycystic Kidney Disease, Adult Type
|
Adpkd
|
|
Polycystic Kidney Diseases
|
Polycystic Kidney, Autosomal Dominant
|
|
Congenital Biliary Ectasias
|
Polycystic Kidney And Hepatic Disease 1
|
|
Polycystic Kidney Disease, Autosomal Dominant
|
Kidney, Polycystic, Disease, Autosomal Dominant
|
|
Adult Polycystic Kidney Disease
|
Polycystic Kidney, Adult Type
|
|
Apckd - [Autosomal Polycystic Kidney Disease]
|
|
|
| Sickle Cell Anemia |
|
Hemoglobin Sc Disease
|
Anemia, Sickle Cell
|
|
Hbsc Disease
|
Sickle Cell-Hemoglobin C Disease Syndrome
|
|
Hb Ss Disease
|
Sickle Cell Trait
|
|
Drepanocytosis
|
Haemoglobin Sc Disease
|
|
Hb Sc Disease
|
Hb-S/Hb-C Disease
|
|
Hb-Ss Disease Without Crisis
|
Hemoglobin S Disease Without Crisis
|
|
Sickle Cell Anaemia
|
Sickle-Cell/Hb-C Disease Without Crisis
|
|
Sickle Cell - Hemoglobin C Disease
|
Hbs Disease
|
|
Hemoglobin S Disease
|
Sickling Disorder Due To Hemoglobin S
|
|
SKCA
|
Sickle Cell Disease
|
|
Sickle Cell-Hemoglobin C Disease
|
Sickle-Cell Disease Carrier
|
|
Sickle-Cell Heterozygous Disorder
|
Haemoglobin A-S Genotype
|
|
Hb-S - [Sickle Cell Haemoglobin] Carrier
|
Sickle Cell Haemoglobin Trait
|
|
As - [Sickle Cell Trait]
|
Hbas - [Sickle Cell Haemoglobin Trait]
|
|
Sickle-Cell Trait Haemoglobin Disease
|
Haemoglobin Sickle Cell Trait Disorder
|
|
Heterozygous Sickle Cell Trait
|
Hbas - [Heterozygous Haemoglobin S]
|
|
|
| Intestinal Pseudo-Obstruction |
|
Chronic Intestinal Pseudoobstruction
|
Chronic Intestinal Pseudo-Obstruction
|
|
Cipo
|
Neuronal Intestinal Dysplasia
|
|
Hollow Visceral Myopathy
|
Familial Visceral Neuropathy
|
|
Paralytic Ileus
|
Intestinal Pseudoobstruction
|
|
Chronic Idiopathic Intestinal Pseudo-Obstruction
|
Ciip
|
|
Congenital Short Bowel Syndrome
|
Enteric Neuropathy
|
|
Familial Visceral Myopathy
|
Ipo
|
|
Pseudo-Obstruction Of Intestine
|
Pseudointestinal Obstruction Syndrome
|
|
Pseudoobstructive Syndrome
|
Congenital Idiopathic Intestinal Pseudoobstruction
|
|
Visceral Myopathy, Familial
|
|
|
| Dubin-Johnson Syndrome |
|
DJS
|
Chronic Idiopathic Jaundice
|
|
Jaundice, Chronic Idiopathic
|
Hyperbilirubinemia, Dubin-Johnson Type
|
|
Hyperbilirubinemia Ii
|
Hyperbilirubinemia Type 2
|
|
Conjugated Hyperbilirubinemia
|
Dubin-Sprinz Disease
|
|
Sprinz-Nelson Syndrome
|
Hblrdj
|
|
Dubin Johnson Syndrome
|
Hyperbilirubinemia 2
|
|
Black Liver-Jaundice Syndrome
|
Chronic Idiopathic Jaundice With Pigmented Liver
|
|
Dubin-Sprinz Syndrome
|
Hyperbilirubinaemia Type 2
|
|
Djs - [Dubin-Johnson Syndrome]
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Nephrogenic Diabetes Insipidus |
|
Vasopressin-Resistant Diabetes Insipidus
|
Diabetes Insipidus, Nephrogenic
|
|
Diabetes Insipidus Nephrogenic
|
Congenital Nephrogenic Diabetes Insipidus
|
|
Adh Resistant Diabetes Insipidus
|
Diabetes Insipidus Nephrogenic X-Linked
|
|
Diabetes Insipidus Nephrogenic Type 1
|
Adh-Resistant Diabetes Insipidus
|
|
Diabetes Insipidus Renalis
|
Ndi
|
|
Renal Diabetes Insipidus
|
Familial Nephrogenic Diabetes
|
|
Antidiuretic-Hormone-Resistant Diabetes Insipidus
|
Adiuretin-Resistant Diabetes Insipidus
|
|
Ndi - [Nephrogenic Diabetes Insipidus]
|
Diabetes Tenuifluus
|
|
Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus
|
Hereditary Nephrogenic Diabetes Insipidus
|
|
Familial Nephrogenic Diabetes Insipidus
|
Primary Nephrogenic Diabetes Insipidus
|
|
|
| Pancreatitis |
|
|
| Intussusception |
|
Intussusception Of Intestine
|
Invagination Of Intestine Or Colon
|
|
|
| Progressive Familial Intrahepatic Cholestasis |
|
Abcb4-Related Intrahepatic Cholestasis
|
Cholestasis, Progressive Familial Intrahepatic
|
|
Pfic
|
Byler Disease
|
|
Abcb11-Related Intrahepatic Cholestasis
|
Atp8b1-Related Intrahepatic Cholestasis
|
|
Bsep Deficiency
|
Byler Disease
|
|
Byler Syndrome
|
Fic1 Deficiency
|
|
Low Γ-Gt Familial Intrahepatic Cholestasis
|
Mdr3 Deficiency
|
|
Pfic
|
Cholestasis, Intrahepatic, Familial, Progressive
|
|
Pfic - [Progressive Familial Intrahepatic Cholestasis]
|
|
|
| Aspergillosis |
|
Aspergillosis, Susceptibility To
|
Infection Due To Aspergillus
|
|
Aspergilloma
|
Aspergillus Nodule
|
|
Simple Aspergilloma
|
Aspergillus
|
|
Aspergillus Flavus Infection
|
Aspergillus Fumigatus Infection
|
|
Aspergillus Infection
|
Infection By Aspergillus Fumigatus
|
|
Intracavitary Aspergillus Fungus Ball
|
Aspergillus Terreus
|
|
|
| Secretory Diarrhea |
|
|
| Acrokeratoderma, Hereditary Papulotranslucent |
|
Hereditary Papulotranslucent Acrokeratoderma
|
|
|
| Methylmalonic Aciduria And Homocystinuria, Cbld Type |
|
Homocystinuria, Cbld Type, Variant 1
|
Methylmalonic Aciduria And Homocystinuria Type Cbld
|
|
Vitamin B12-Responsive Methylmalonic Acidemia, Type Cbldv2
|
MAHCD
|
|
Methylmalonic Acidemia And Homocystinuria, Cbld Type
|
Methylmalonic Aciduria, Cblh Type, Formerly
|
|
Methylmalonic Acidemia, Cblh Type, Formerly
|
Methylmalonic Aciduria, Cbld Type, Variant 2
|
|
Cobalamin D Deficiency
|
Methylcobalamin Deficiency Type Cbldv1
|
|
Functional Methionine Synthase Deficiency Type Cbldv1
|
Vitamin B12-Responsive Methylmalonic Aciduria, Type Cbldv2
|
|
Methylmalonic Acidemia With Homocystinuria, Type Cbld
|
Cbld Defect
|
|
Cobalamin D Defect
|
Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cbld
|
|
Methylmalonic Aciduria With Homocystinuria, Type Cbld
|
Homocystinuria Cbld Variant 1
|
|
Methylmalonic Acidemia And Homocystinuria Cbld Type
|
Methylmalonic Aciduria And Homocystinuria Cbld-Combined
|
|
Methylmalonic Aciduria And Homocystinuria Cbld Original
|
Methylmalonic Aciduria Cbld Variant 2
|
|
Aciduria, Methylmalonic, And Homocystinuria, Cbld Type
|
|
|
| Microvillus Inclusion Disease |
|
Congenital Microvillous Atrophy
|
Intractable Diarrhea Of Infancy
|
|
Congenital Familial Protracted Diarrhea With Enterocyte Brush-Border Abnormalities
|
Davidson Disease
|
|
Congenital Microvillus Atrophy
|
Microvillous Inclusion Disease
|
|
Mvid
|
Diarrhea 2 With Microvillus Atrophy
|
|
Mvd
|
Congenital Familial Protracted Diarrhea
|
|
Davidson'S Disease
|
Familial Enteropathy, Microvillus
|
|
Microvillus Atrophy, Congenital
|
Congenital Enteropathy
|
|
Familial Protracted Enteropathy
|
Microvillous Atrophy
|
|
Microvillus Atrophy With Diarrhea 2
|
Idi
|
|
|
| Constipation |
|
|
| Cholangitis |
|
Acute Cholangiolitis
|
Ascending Cholangitis
|
|
Cholangiolitis
|
Cholangitis Nos
|
|
Chronic Cholangiolitis
|
Hepatic Duct Inflammation
|
|
Acute Cholangitis
|
Bile Duct Inflammation
|
|
|
| Cholestasis, Benign Recurrent Intrahepatic, 1 |
|
Benign Recurrent Intrahepatic Cholestasis
|
BRIC1
|
|
Summerskill Syndrome
|
Bric
|
|
Summerskill-Walshe-Tygstrup Syndrome
|
Cholestasis, Benign Recurrent Intrahepatic
|
|
Benign Recurrent Intrahepatic Cholestasis 1
|
Benign Recurrent Intrahepatic Cholestasis Type 1
|
|
Bric Type 1
|
Low Gamma-Gt Familial Intrahepatic Cholestasis
|
|
Recurrent Familial Intrahepatic Cholestasis
|
Cholestasis, Benign Recurrent Intrahepatic 1
|
|
Mild Atp8b1 Deficiency
|
Recurrent Familial Intrahepatic Cholestasis 1
|
|
Abcb11-Related Intrahepatic Cholestasis
|
Atp8b1-Related Intrahepatic Cholestasis
|
|
Cholestasis, Intrahepatic, Recurrent, Benign, Type 1
|
Progressive Intrahepatic Cholestasis
|
|
Cholestasis, Progressive Familial Intrahepatic 3
|
Bric - [Benign Recurrent Intrahepatic Cholestasis]
|
|
|
| Alcoholic Pancreatitis |
|
Pancreatitis, Alcoholic
|
Pancreatitis Alcoholic
|
|
|
| Urea Cycle Disorder |
|
Urea Cycle Disorders
|
Urea Cycle Disorders, Inborn
|
|
Disorder Of Metabolism Of Ornithine, Citrulline, Argininosuccinic Acid, Arginine And Ammonia
|
Disorder Of Urea Cycle Metabolism
|
|
Urea Cycle Defect
|
Ucd
|
|
Disorder Of The Urea Cycle Metabolism
|
Disorder Of Urea Cycle
|
|
Disorders Of Metabolism Of Ornithine, Citrulline, Argininosuccinic Acid, Arginine And Ammonia
|
Ammonia Metabolic Disorder
|
|
|
| Cholangitis, Primary Sclerosing |
|
Primary Sclerosing Cholangitis
|
PSC
|
|
Sclerosing Cholangitis
|
Cholangitis, Sclerosing
|
|
Cholangitis Primary Sclerosing
|
Psc - [Primary Sclerosing Cholangitis]
|
|
|
| Gallbladder Disease |
|
Gallbladder Diseases
|
Gall Bladder
|
|
Gall Bladder Diseases
|
Abnormal Gallbladder Function
|
|
|
| Cryptorchidism, Unilateral Or Bilateral |
|
Cryptorchidism
|
Undescended Testicle
|
|
Undescended Testis
|
Cryptorchism
|
|
Undescended Testicles
|
CRYPTO
|
|
Impaired Testicular Descent
|
Cryptosporidiosis
|
|
Retained Testis
|
Unilateral Cryptorchidism
|
|
Unilateral Undescended Testis
|
Nondescent Unilateral Testicle
|
|
Unilateral Cryptorchism
|
Ectopic Testis, Unilateral
|
|
Bilateral Cryptorchidism
|
Bilateral Cryptorchism
|
|
Bilateral Nondescent Testicle
|
Bilateral Undescended Testes
|
|
Bilateral Ectopic Testes
|
|
|
| Hypogonadotropic Hypogonadism |
|
Klinefelter Syndrome
|
Klinefelter'S Syndrome
|
|
Xxy Syndrome
|
Xxy Trisomy
|
|
Hypogonadotropism
|
47, Xxy
|
|
Congenital Idiopathic Hypogonadotropic Hypogonadism
|
Isolated Congenital Gonadotropin Deficiency
|
|
47,Xxy Syndrome
|
47, Xxy Syndrome
|
|
Klinefelters Syndrome
|
Hypogonadism
|
|
Klinefelter Syndrome In Males
|
Klinefelter Syndrome, Unspecified
|
|
Klinefelter Syndrome Karyotype 47, Xxy
|
|
|
| Male Infertility With Azoospermia Or Oligozoospermia Due To Single Gene Mutation |
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Familial Pancreatic Carcinoma
|
|
Pancreatic Neoplasm
|
Carcinoma Of Pancreas
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm 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
|
|
Cancer Of The Pancreas
|
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
|
|
|
| Asthma |
|
Chronic Obstructive Asthma
|
Asthma, Diminished Response To Antileukotriene Treatment In
|
|
Bronchial Hyperreactivity
|
Asthma, Susceptibility To
|
|
Asthma, Bronchial
|
Asthma, Protection Against
|
|
Asthma, Nocturnal, Susceptibility To
|
Nocturnal Asthma
|
|
Asthma-Related Traits
|
Asthma-Related Traits, Susceptibility To
|
|
Asthma, Nocturnal
|
Chronic Obstructive Asthma With Acute Exacerbation
|
|
Chronic Obstructive Asthma With Status Asthmaticus
|
Exercise Induced Asthma
|
|
Exercise-Induced Asthma
|
Bronchial Asthma
|
|
Asthma, Exercise-Induced
|
Idiosyncratic Asthma
|
|
Unspecified Asthma With Acute Exacerbation
|
Asthma, Unspecified, With Stated Status Asthmaticus
|
|
Status Asthmaticus Nos
|
Acute Severe Asthma
|
|
Acute Severe Bronchial Asthma
|
Status Asthma
|
|
Status Post Asthmaticus
|
|
|
| Oligospermia |
|
|
| Idiopathic Bronchiectasis |
|
|
| Plasma Protein Metabolism Disease |
|
|
| Autosomal Genetic Disease |
|
Autosomal Hereditary Disorder
|
|
|
| Polycystic Liver Disease |
|
Autosomal Dominant Polycystic Liver Disease
|
Isolated Polycystic Liver Disease
|
|
Pcld
|
Congenital Cystic Liver Disease
|
|
Congenital Hepatic Cyst
|
Fibrocystic Liver Disease
|
|
Isolated Autosomal Dominant Polycystic Liver Disease
|
Adpcld
|
|
Liver Disease, Polycystic
|
Multiple Cysts Of Liver
|
|
Pld - [Polycystic Liver Disease]
|
Polycystic Liver Disorder
|
|
Polycystic Liver
|
Congenital Polycystic Disease Of Liver
|
|
Congenital Polycystic Liver Disease
|
|
|
| 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
|
|
|
| Autosomal Recessive Disease |
|
Autosomal Recessive Disorder
|
|
|
| Male Infertility |
|
Infertility, Male
|
Infertility Male
|
|
Male Sterility
|
Absolute Infertility
|
|
|
| Renal Hypodysplasia/Aplasia 1 |
|
Renal Agenesis
|
Renal Adysplasia
|
|
Renal Aplasia
|
RHDA1
|
|
Hereditary Renal Aplasia
|
Hra
|
|
Hereditary Urogenital Adysplasia
|
Hypodysplasia/Aplasia, Renal, Type 1
|
|
Congenital Absence Of Kidneys Syndrome
|
Congenital Absence Of Kidney
|
|
Aplastic Kidney
|
|
|
| Spermatogenic Failure |
|
Azoospermia
|
Spgf
|
|
Spermatogenic Failure, Susceptibility To
|
Absent Sperm
|
|
Aspermatogenesis
|
Infertility Due To Azoospermia
|
|
Hypospermatogenesis
|
Azoospermatism
|
|
|
| Typhoid Fever |
|
Typhoid
|
Enteric Fever
|
|
Typhoidal Salmonellosis
|
Ileotyphus
|
|
Infection By Salmonella Typhi
|
Typhoid Any Site
|
|
Typhoid Fever Any Site
|
Typhoid Infection
|
|
Typhoid Infection Any Site
|
Typhoid Fever Confirmed
|
|
Enteric Fever Nos
|
|
|
| Pancreatitis, Hereditary |
|
Hereditary Pancreatitis
|
Chronic Pancreatitis
|
|
Hereditary Chronic Pancreatitis
|
Hp
|
|
Pancreatitis, Chronic, Susceptibility To
|
PCTT
|
|
Hpc
|
Pancreatitis, Chronic
|
|
Pancreatitis, Chronic, Protection Against
|
Autosomal Dominant Hereditary Pancreatitis
|
|
Familial Pancreatitis
|
Cp
|
|
Pancreatitis Hereditary
|
|
|
| Allergic Bronchopulmonary Aspergillosis |
|
Aspergillosis, Allergic Bronchopulmonary
|
Abpa
|
|
Allergic Bronchopulmonary Mycosis
|
Hinson-Pepys Disease
|
|
Pulmonary Aspergillus Disease
|
Allergic Aspergillosis
|
|
Aspergillosis Allergic Bronchopulmonary
|
|
|
| Spermatocele |
|
|
| Autoimmune Pancreatitis |
|
Lymphoplasmocytic Sclerosing Pancreatitis
|
Aip
|
|
|
| Exocrine Pancreatic Insufficiency |
|
|
| Bronchiectasis |
|
Polynesian Bronchiectasis
|
Kartagener Syndrome
|
|
Bronchiectasis Nos
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Paranasal Sinus Disease |
|
Paranasal Sinus Diseases
|
Disorder Of Nasal Sinus
|
|
|
| Pseudohypoaldosteronism |
|
|
| Muscular Dystrophy |
|
Muscular Dystrophies
|
Congenital Md
|
|
Congenital Muscular Dystrophy
|
Cmd
|
|
Mdc
|
Dystrophy, Muscular
|
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
| Lung Disease |
|
Lung Diseases
|
Disorder Of Lung
|
|
Abnormality Of The Lung
|
|
|
| Nuchal Bleb, Familial |
|
Fetal Cystic Hygroma
|
Cystic Hygroma, Fetal
|
|
Fch
|
Lymphangioma, Cystic
|
|
|
| Phenylketonuria |
|
Phenylalanine Hydroxylase Deficiency
|
PKU
|
|
Pah Deficiency
|
Folling Disease
|
|
Maternal Phenylketonuria
|
Phenylketonurias
|
|
Oligophrenia Phenylpyruvica
|
Hyperphenylalaninemia, Non-Pku Mild
|
|
Folling'S Disease
|
Phenylalaninemia
|
|
Mild Phenylketonuria
|
Mild Pku
|
|
Variant Pku
|
Variant Phenylketonuria
|
|
Mpku
|
Phenylketonuria, Maternal
|
|
Deficiency Disease, Phenylalanine Hydroxylase
|
Phenylalanine Hydroxylase Deficiency Disease
|
|
Hyperphenylalaninemic Embryopathy
|
Maternal Pku
|
|
Maternal Hyperphenylalaninemia
|
Phenylketonuric Embryopathy
|
|
Hyperphenylalaninemia
|
HPA
|
|
Non-Phenylketonuria Hyperphenylalaninemia
|
NON-PKU HPA
|
|
Phenylketonuria Maternal
|
Classical Phenylketonuria
|
|
Hyperphenylalaninaemia
|
Pku - [Phenylketonuria]
|
|
|
| Tuberculous Epididymitis |
|
Tuberculosis Of Epididymis
|
|
|
| Kartagener Syndrome |
|
|
| Chronic Ethmoiditis |
|
Chronic Ethmoidal Sinusitis
|
Chronic Ethmoid Sinusitis
|
|
Ethmoidal Sinusitis - Chronic
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Aquagenic Syringeal Acrokeratoderma |
|
Aquagenic Palmoplantar Keratoderma
|
Aquagenic Keratoderma
|
|
Aquagenic Wrinkling Of The Palms
|
Transient Reactive Papulotranslucent Acrokeratoderma
|
|
Aquagenic Wrinkling Of The Hands
|
|
|
| Pancreas Disease |
|
Abnormality Of The Pancreas
|
Pancreatic Diseases
|
|
|
| Biliary Dyskinesia |
|
Sphincter Of Oddi Dysfunction
|
|
|
| Primary Ciliary Dyskinesia |
|
Immotile Cilia Syndrome
|
Kartagener Syndrome
|
|
Dextrocardia Bronchiectasis And Sinusitis
|
Pcd
|
|
Ciliary Motility Disorders
|
Ciliary Motility Disorder
|
|
Immotile Ciliary Syndrome
|
Ciliary Dyskinesia Primary
|
|
Ics
|
Polynesian Bronchiectasis
|
|
Dextrocardia-Bronchiectasis-Sinusitis Syndrome
|
Immotile Cilia Syndrome, Kartagener Type
|
|
Primary Ciliary Dyskinesia And Situs Inversus
|
Primary Ciliary Dyskinesia, Kartagener Type
|
|
Siewert Syndrome
|
Dyskinesia, Ciliary, Primary
|
|
|
| Mucopolysaccharidosis-Plus Syndrome |
|
Mucopolysaccharidosis
|
Mucopolysaccharidosis-Like Syndrome With Congenital Heart Defects And Hematopoietic Disorders
|
|
MPSPS
|
Mucopolysaccharidoses
|
|
Mps
|
Mucopolysaccharidosis-Like Plus Disease
|
|
Disorders Of Glycosaminoglycan Metabolism
|
|
|
| Inflammatory Diarrhea |
|
|
| Pseudohypoaldosteronism, Type I, Autosomal Recessive |
|
Autosomal Recessive Pseudohypoaldosteronism Type 1
|
PHA1B
|
|
Pseudohypoaldosteronism Type 1
|
Pseudohypoaldosteronism, Type I
|
|
Generalized Pha1
|
Generalized Pseudohypoaldosteronism Type 1
|
|
Pseudohypoaldosteronism Type 1 Autosomal Recessive
|
Pha1
|
|
Pseudohypoaldosteronism
|
Pha I, Autosomal Recessive
|
|
Autosomal Recessive Pha 1
|
Pseudohypoaldosteronism Type 1, Recessive
|
|
Pseudohypoaldosteronism Type I
|
Autosomal Recessive Pha1
|
|
Pha Type 1
|
Pseudohypoaldosteronism 1, Autosomal Recessive
|
|
Multisystem Pseudohypoaldosteronism
|
Pha Type I, Autosomal Recessive
|
|
Pseudohypoaldosteronism Type I, Autosomal Recessive
|
|
|
| Tay-Sachs Disease |
|
Hexosaminidase A Deficiency
|
TSD
|
|
Hexa Deficiency
|
Gm2 Gangliosidosis, Type 1
|
|
Hexosaminidase Alpha-Subunit Deficiency
|
Gm2-Gangliosidosis, Several Forms
|
|
Gm2-Gangliosidosis, B, B1, Ab Variant
|
B Variant Gm2 Gangliosidosis
|
|
Sphingolipidosis, Tay-Sachs
|
Gm2-Gangliosidosis, Type I
|
|
B Variant Gm2-Gangliosidosis
|
Hex A Pseudodeficiency
|
|
Hexa Disorders
|
Beta-Hexosaminidase A Deficiency
|
|
Gm2 Gangliosidosis, Type I
|
Gangliosidosis Gm2 , Type 1
|
|
Gm2 Gangliosidosis, B, B1 Variant
|
Gm2-Gangliosidosis 1
|
|
GM2G1
|
Gm2-Gangliosidosis B Variant
|
|
Tay-Sachs Disease Pseudo-Ab Variant
|
Tay-Sachs Disease Variant B1
|
|
Gangliosidoses, Gm2
|
|
|
| Ileus |
|
|
| Duodenal Atresia |
|
Duodenal Stenosis
|
Familial Duodenal Atresia
|
|
|
| Bronchiectasis With Or Without Elevated Sweat Chloride 1 |
|
Bronchiectasis With Or Without Elevated Sweat Chloride 1, Modifier Of
|
BESC1
|
|
Cystic Fibrosis-Like Syndrome
|
Bronchiectasis, With/Without Elevated Sweat Chloride, Type 1, Modifier Of
|
|
|
| Cholera |
|
Vibrio Cholerae Infection
|
Cholera - Vibrio Cholerae
|
|
Cholera Due To Vibrio Cholerae
|
Vibrio Cholerae
|
|
Cholera Syndrome
|
Asiatic Cholera
|
|
Epidemic Cholera
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Interstitial Lung Disease 2 |
|
Idiopathic Pulmonary Fibrosis
|
Ipf
|
|
Fibrocystic Pulmonary Dysplasia
|
Pulmonary Fibrosis, Idiopathic
|
|
Pulmonary Fibrosis, Idiopathic, Susceptibility To
|
ILD2
|
|
Idiopathic Pulmonary Fibrosis, Familial
|
Fibrosing Alveolitis, Cryptogenic
|
|
Uip
|
Cryptogenic Fibrosing Alveolitis
|
|
Fibrosing Alveolitis
|
Interstitial Pneumonitis, Usual
|
|
Familial Idiopathic Pulmonary Fibrosis
|
Idiopathic Fibrosing Alveolitis, Chronic Form
|
|
Usual Interstitial Pneumonia
|
Fibrosing Alveolitis Cryptogenic
|
|
Hamman-Rich Disease
|
Idiopathic Pulmonary Fibrosis Familial
|
|
Interstitial Pneumonitis Usual
|
Fibrosis Idiopathic Pulmonary
|
|
Fibrosis, Pulmonary, Idiopathic
|
Hamman-Rich Syndrome
|
|
Chronic Idiopathic Pulmonary Fibrosis
|
Acute Interstitial Pneumonia
|
|
Interstitial Pulmonary Fibrosis
|
Ipf - [Idiopathic Pulmonary Fibrosis]
|
|
Idiopathic Lung Fibrosis
|
Fibrosing Lung Disease
|
|
Pulmonary Fibrosis Nos
|
Fibrosing Pneumonitis
|
|
|
| Intestinal Obstruction |
|
Inspissated Milk Syndrome
|
Milk Curd Syndrome
|
|
|
| Prss1-Related Hereditary Pancreatitis |
|
|
| Diabetes Mellitus |
|
|
| Pulmonary Edema |
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Respiratory Failure |
|
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
|
Acute And Chronic Respiratory Failure
|
Respiratory Insufficiency/Failure
|
|
Chronic Respiratory Disease
|
Respiratory Disease
|
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
|
Respiration Disorders
|
Respiratory Tract Diseases
|
|
Lung Failure Nos
|
Pulmonary Failure
|
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
|
Chronic Respiration Failure
|
|
|
| Infertility |
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Vas Deferens, Congenital Bilateral Aplasia Of, X-Linked |
|
CBAVDX
|
Congenital Bilateral Absence Of Vas Deferens, X-Linked
|
|
X-Linked Congenital Bilateral Absence Of Vas Deferens
|
Congenital Bilateral Aplasia Of The Vas Deferens, X-Linked
|
|
Male Urogenital Diseases
|
|
|
| Liddle Syndrome 1 |
|
Liddle Syndrome
|
Pseudoaldosteronism
|
|
LIDLS1
|
Lidls
|
|
Pseudohyperaldosteronism
|
Liddle'S Syndrome
|
|
Pseudoprimary Hyperaldosteronism
|
Pseudohyperaldosteronism Type 1
|
|
Liddles Syndrome
|
|
|
| Pneumonia |
|
Acute Pneumonia
|
Pneumonias
|
|
Infectious Pneumonia
|
Pn - [Pneumonia]
|
|
Lobar Pneumonia Nos
|
Multifocal Pneumonia
|
|
Orthostatic Pneumonia
|
Pneumonia Nos
|
|
Chronic Pneumonia Nos
|
Atypical Pneumonia
|
|
Passive Pneumonia
|
Purulent Pneumonia
|
|
Interstitial Lobar Pneumonia
|
Pneumonia, Unspecified
|
|
Pneumonia Due To Chlamydia
|
Pneumonia Due To Chlamydia Pneumoniae
|
|
Pneumonia Due To E. Coli
|
Escherichia Coli Lobar Pneumonia
|
|
Pneumonia Due To H. Influenzae
|
Pneumonia Due To Hemophilus Influenzae
|
|
Bronchopneumonia Due To H. Influenzae
|
Haemophilus Influenzae Lobar Pneumonia
|
|
Bronchopneumonia Due To Hemophilus Influenzae
|
Pseudomonal Pneumonia
|
|
Pseudomonas Pneumonia
|
Pseudomonas Lobar Pneumonia
|
|
Staphylococcal Pneumonia
|
Staphylococcus Pneumonia
|
|
Acute Staphylococcal Pneumonia
|
Staphylococcal Double Pneumonia
|
|
Staphylococcal Lobar Pneumonia
|
Staphylococcal Purulent Pneumonia
|
|
Staphylococcal Bronchopneumonia
|
Pneumococcal Pneumonia
|
|
Pneumococcus Pneumonia
|
Bronchopneumonia Due To S. Pneumoniae
|
|
Pneumococcal Lobar Pneumonia
|
Streptococcal Pneumoniae Pneumonia
|
|
Streptococcus Pneumoniae Lobar Pneumonia
|
Pyemic Pneumococcal Embolism With Pneumonia
|
|
Bronchopneumonia Due To Streptococcus Pneumoniae
|
Pneumonia Due To Streptococcus, Group B
|
|
Group B Streptococcal Pneumonia
|
Adenovirus Pneumonia
|
|
Adenoviral Pneumonia
|
Adenovirus Viral Pneumonia
|
|
Pneumonia Respiratory Syncytial Viral
|
Parainfluenza Viral Pneumonia
|
|
Parainfluenzal Pneumonia
|
Parainfluenza Virus Pneumonia
|
|
Human Metapneumovirus Pneumonia
|
Human Metapneumovirus Infection Resulting In Pneumonia
|
|
Pneumocystis Pneumonia
|
Plasma Cells Pneumonia
|
|
|
| Cholestasis, Intrahepatic, Of Pregnancy 3 |
|
ICP3
|
Cholestasis, Intrahepatic, Of Pregnancy, 3
|
|
Intrahepatic Cholestasis Of Pregnancy 3
|
Pregnancy Related Cholestasis 3
|
|
Cholestasis Of Pregnancy, Intrahepatic 3
|
Cholestasis, Intrahepatic, Of Pregnancy, Type 3
|
|
|
