| Diseases |
Alias |
|
| Hypoparathyroidism |
|
Hypoparathyroidism, Idiopathic
|
Parathyroid, Underactivity Of
|
|
Syndrome With Hypoparathyroidism
|
Deficiency Of Parathyroid Hormone
|
|
Parathyroid Gland Insufficiency
|
Parathyroid Insufficiency
|
|
Hypoparathyroidism Due To Impaired Pth - [Parathyroid Hormone] Secretion
|
|
|
| Hyperparathyroidism |
|
Hyperparathyroidism And Other Disorders Of Parathyroid Gland
|
Parathyroid Hyperfunction
|
|
Hpth - [Hyperparathyroidism]
|
Parathyroid Gland Hyperfunction
|
|
Parathyroid Glandular Hyperfunction
|
|
|
| Insulinoma |
|
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
| 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
|
|
|
| Hypoparathyroidism-Retardation-Dysmorphism Syndrome |
|
Sanjad-Sakati Syndrome
|
Hrd Syndrome
|
|
HRDS
|
Hypoparathyroidism-Intellectual Disability-Dysmorphism Syndrome
|
|
Hypoparathyroidism-Short Stature-Intellectual Disability-Seizures Syndrome
|
Richardson-Kirk Syndrome
|
|
Sss
|
Hypoparathyroidism With Short Stature, Mental Retardation, And Seizures
|
|
Hypoparathyroidism, Congenital, Associated With Dysmorphism, Growth Retardation, And Developmental Delay
|
Hypoparathyroidism With Short Stature, Mental Retardation And Seizures
|
|
Hypoparathyroidism With Short Stature, Intellectual Disability And Seizures
|
Hypoparathyroidism, Congenital, Associated With Dysmorphism, Growth Retardation And Developmental Delay
|
|
|
| Gastrinoma |
|
Gastrin Cell Tumour
|
Gastrin Secreting Tumor
|
|
Malignant Gastrinoma
|
Gastrinoma, Malignant
|
|
|
| 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
|
|
|
| 17-Beta Hydroxysteroid Dehydrogenase Iii Deficiency |
|
17-Ksr Deficiency
|
Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency
|
|
Pseudohermaphroditism, Male, With Gynecomastia
|
17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency
|
|
Testosterone 17-Beta-Dehydrogenase Deficiency
|
17-Ketosteroid Reductase Deficiency Of Testis
|
|
17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
|
17-Ketoreductase Deficiency
|
|
17-Ketosteroidreductase Deficiency
|
46,Xy Disorder Of Sex Development Due To 17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
|
|
Male Pseudohermaphroditism With Gynecomastia
|
17 Alpha Ksr Deficiency
|
|
17 Alpha Ketosteroid Reductase Deficiency Of Testis
|
17 Beta Hydroxysteroid Dehydrogenase Iii Deficiency
|
|
Male Pseudoherma-Phroditism With Gynecomastia
|
Neutral 17 Beta Hydroxysteroid Oxidoreductase Deficiency
|
|
Male Pseudohermaphrodism With Gynecomastia
|
MPH
|
|
17-Hydroxysteroid Dehydrogenase Deficiency
|
|
|
| Pulmonary Hypertension |
|
Primary Pulmonary Hypertension
|
Hypertension Pulmonary
|
|
Hypertension, Pulmonary
|
Idiopathic Pulmonary Hypertension
|
|
Idiopathic Pulmonary Arterial Hypertension
|
Pulmonary Htn - [Hypertension]
|
|
|
| Phosphorus Metabolism Disease |
|
Phosphorus Metabolism Disorders
|
Disorder Of Phosphorus Metabolism
|
|
Phosphorus Disorder
|
Phosphorus Metabolism Disorder
|
|
|
| Bone Disease |
|
Bone Diseases
|
Skeletal Disease
|
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
| Chondrocalcinosis |
|
Pseudogout
|
Calcium Pyrophosphate Deposition Disease
|
|
Familial Chondrocalcinosis
|
Chondrocalcinosis Nos
|
|
Cppd - [Calcium Pyrophosphate Deposition Disease]
|
Cpdd - [Calcium Pyrophosphate Deposition Disease]
|
|
Chondrocalcinosis, Due To Pyrophosphate Crystals, Involving Unspecified Site
|
Chondrocalcinosis, Cause Unspecified
|
|
Chondrocalcinosis Due To Pyrophosphate Crystals
|
Chondrocalcinosis Articularis
|
|
Calcium Pyrophosphate Arthritis And Periarthritis
|
|
|
| Autoimmune Polyendocrine Syndrome, Type I, With Or Without Reversible Metaphyseal Dysplasia |
|
APS1
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
|
|
Apeced
|
Pga I
|
|
Hypoadrenocorticism With Hypoparathyroidism And Superficial Moniliasis
|
Autoimmune Polyendocrinopathy Syndrome , Type I, With Or Without Reversible Metaphyseal Dysplasia
|
|
Polyglandular Autoimmune Syndrome, Type 1
|
Autoimmune Polyglandular Syndrome Type 1
|
|
Autoimmune Polyendocrine Syndrome Type 1
|
Autoimmune Polyendocrinopathy Syndrome Type 1
|
|
Whitaker Syndrome
|
Aps Type 1
|
|
Polyglandular Type I Autoimmune Syndrome
|
Aps I
|
|
Autoimmune Polyglandular Syndrome, Type I
|
Polyglandular Autoimmune Syndrome, Type I
|
|
Aps 1
|
Autoimmune Polyglandular Syndrome Type I
|
|
Pga 1
|
Pga-I
|
|
Polyglandular Autoimmune Syndrome Type 1
|
Type I Polyglandular Autoimmune Syndrome
|
|
Aire Deficiency
|
Autoimmune Polyendocrinopathy With Candidiasis And Ectodermal Dystrophy
|
|
Autoimmune Polyglandular Syndrome, Type 1
|
Autoimmune Polyendocrinopathy Type 1
|
|
Apeced Syndrome
|
Autoimmune Hypoparathyroidism-Chronic Candidiasis-Addison Disease Syndrome
|
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome
|
Ham Syndrome
|
|
Hypoparathyroidism-Addison Disease-Mucocutaneous Candidiasis Syndrome
|
Medac Syndrome
|
|
Multiple Endocrine Deficiency-Addison Disease-Candidiasis Syndrome
|
Autoimmune Polyendocrine Syndrome 1, With Or Without Reversible Metaphyseal Dysplasia
|
|
Aps-1
|
Autoimmune Polyendocrine Syndrome Type I
|
|
Autoimmune Polyendocrinopathy Syndrome Type I
|
Autosomal Dominant Autoimmune Polyendocrinopathy Syndrome Type I
|
|
Polyglandular Autoimmune Syndrome Type I
|
Polyglandular Deficiency Syndrome Persian-Jewish Type
|
|
Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
|
Polyendocrinopathy Autoimmune, Type 1, With/Without Reversible Metaphyseal Dysplasia
|
|
|
| Metal Metabolism Disorder |
|
Metal Metabolism, Inborn Errors
|
Inborn Metal Metabolism Disorder
|
|
|
| Hyperparathyroidism, Neonatal Severe |
|
NSHPT
|
Neonatal Severe Primary Hyperparathyroidism
|
|
Nsph
|
Nhpt
|
|
Hyperparathyroidism, Neonatal
|
Hyperparathyroidism, Neonatal Severe Primary
|
|
Neonatal Severe Hyperparathyroidism
|
Hyperparathyroidism, Severe, Neonatal
|
|
Neonatal Hyperparathyroidism
|
|
|
| Parathyroid Adenoma |
|
Adenoma Of Parathyroid
|
Adenoma Of The Parathyroid Gland
|
|
Parathyroid Gland Adenoma
|
|
|
| Hypercalcemia, Infantile, 1 |
|
HCINF1
|
Hypercalcemia, Idiopathic, Of Infancy
|
|
Hypercalcemia Infantile
|
Idiopathic Hypercalcemia Of Infancy
|
|
Infantile Hypercalcemia
|
Hypercalcemia, Infantile
|
|
Hypercalcemia, Infantile, Type 1
|
Hypercalcemia
|
|
|
| Nephrolithiasis |
|
Kidney Stones
|
Stone - Kidney/Ureter
|
|
Kidney Calculi
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| 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 |
|
|
| Renal Tubular Transport Disease |
|
Renal Tubular Transport, Inborn Errors
|
Inborn Renal Tubular Transport Disorder
|
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| Bartter Disease |
|
Bartter Syndrome
|
Bartter'S Syndrome
|
|
Aldosteronism With Hyperplasia Of The Adrenal Cortex
|
Hypokalemic Alkalosis With Hypercalciuria
|
|
Potassium Wasting
|
Juxtaglomerular Hyperplasia With Secondary Aldosteronism
|
|
Renal Tubular Normotensive Hypokalemic Alkalosis With Hypercalciuria
|
Salt-Losing Tubular Disorder, Henle'S Loop Type
|
|
Salt-Wasting Tubulopathy, Henle'S Loop Type
|
Bartters Syndrome
|
|
|
| Hypocalciuric Hypercalcemia, Familial, Type Iii |
|
HHC3
|
Familial Hypocalciuric Hypercalcemia 3
|
|
Fbh3
|
Familial Hypocalciuric Hypercalcemia Type 3
|
|
Hypercalcemia, Familial Benign, Oklahoma Type
|
Hypocalciuric Hypercalcemia, Type Iii
|
|
Fhh Type 3
|
Hypocalciuric Hypercalcemia Type Iii
|
|
Familial Benign Hypercalcemia, Type Iii
|
Hypercalcemia, Familial Benign, Type Iii
|
|
Fbhok
|
Familial Benign Hypercalcemia, Oklahoma Variant
|
|
Familial Benign Hypercalcemia, Type 3
|
Hypercalcemia, Familial Benign, Type 3
|
|
Hypocalciuric Hypercalcemia, Familial, Type 3
|
Hypocalciuric Hypercalcemia, Familial 3
|
|
Familial Benign Hypercalcemia 3
|
Familial Benign Hypercalcemia Oklahoma Type
|
|
Familial Benign Hypocalciuric Hypercalcemia 3
|
Fbhh3
|
|
Fhh3
|
|
|
| Hypocalcemia, Autosomal Dominant 1 |
|
Autosomal Dominant Hypocalcemia
|
Autosomal Dominant Hypocalcemia 1
|
|
HYPOC1
|
Hypocalcemia, Autosomal Dominant
|
|
Hypercalciuric Hypocalcemia
|
Hypocalcemia, Autosomal Dominant, With Bartter Syndrome
|
|
Familial Hypocalcemia
|
Hypocalcemia, Familial
|
|
Hypoc
|
Adh
|
|
Autosomal Dominant Hypoparathyroidism
|
Familial Hypercalciuric Hypocalcemia
|
|
Ad Hypocalcemia
|
Autosomal Dominant Hypocalcemia With Bartter Syndrome
|
|
Hypoparathyroidism - Autosomal Dominant
|
Hypocalcemia
|
|
|
| Hypercalciuria, Absorptive, 2 |
|
HCA2
|
Hypercalciuria, Absorptive, Susceptibility To
|
|
Hypercalciuria, Absorptive
|
Familial Idiopathic Hypercalciuria
|
|
Hypercalciuria, Familial Idiopathic
|
Hypercalciuria Absorptive 2
|
|
Hypercalciuria Familial Idiopathic
|
Hypercalciuria, Absorptive, Type 2
|
|
Hypercalciuria
|
|
|
| Epilepsy, Idiopathic Generalized |
|
Idiopathic Generalized Epilepsy
|
Generalised Epilepsy
|
|
Epilepsy, Generalized
|
EIG
|
|
Ige
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 1
|
|
Epilepsy, Idiopathic Generalized 1
|
Epilepsy, Idiopathic Generalized, Susceptibility To
|
|
Epilepsy, Idiopathic, Generalized
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 1
|
|
|
| Parathyroid Gland Disease |
|
Parathyroid Diseases
|
Disease Of Parathyroid Glands
|
|
Parathyroid Disease
|
|
|
| Familial Isolated Hypoparathyroidism |
|
|
| Urolithiasis |
|
|
| Secondary Hyperparathyroidism |
|
Hyperparathyroidism Secondary
|
Hyperparathyroidism, Secondary
|
|
Secondary Hyperparathyroidism Nec
|
|
|
| Adenoma |
|
Acinar Cell Adenoma
|
Adenomas
|
|
Acinic Cell Adenoma
|
|
|
| Epilepsy, Myoclonic Juvenile |
|
Juvenile Myoclonic Epilepsy
|
Janz Syndrome
|
|
Jme
|
Myoclonic Epilepsy, Juvenile, Susceptibility To, 1
|
|
EJM
|
Myoclonic Epilepsy, Juvenile
|
|
Petit Mal, Impulsive
|
Myoclonic Epilepsy, Juvenile 1
|
|
Myoclonic Epilepsy, Juvenile, 1
|
Adolescent Myoclonic Epilepsy
|
|
Juvenile Myoclonus Epilepsy
|
Juvenile Myoclonic Epilepsy 1
|
|
EJM1
|
Petit Mal Impulsive
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 1
|
Myoclonic Epilepsy Juvenile
|
|
Epilepsy, Myoclonic, Juvenile
|
Myoclonic Epilepsy Of Janz
|
|
Jme - [Juvenile Myoclonic Epilepsy]
|
|
|
| Renal Osteodystrophy |
|
Renal Rickets
|
Chronic Kidney Disease-Mineral And Bone Disorder
|
|
|
| Familial Hypocalciuric Hypercalcemia |
|
Familial Benign Hypercalcemia
|
Fbh
|
|
Fbhh
|
Fhh
|
|
Familial Benign Hypocalciuric Hypercalcemia
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
|
| Hyperparathyroidism 2 With Jaw Tumors |
|
Hyperparathyroidism-Jaw Tumor Syndrome
|
Hpt-Jt
|
|
HRPT2
|
Familial Primary Hyperparathyroidism With Multiple Ossifying Jaw Fibromas
|
|
Parathyroid Adenoma With Cystic Changes
|
Hereditary Hyperparathyroidism-Jaw Tumor Syndrome
|
|
Hyperparathyroidism 2
|
Hyperparathyroidism, Familial Primary, With Multiple Ossifying Jaw Fibromas
|
|
Hyperparathyroidism-Jaw Tumor Syndrome, Hereditary
|
Familial Cystic Parathyroid Adenomatosis
|
|
Hyperparathyroidism-Jaw Tumor Syndrome, Type 2
|
Parathyroid Adenomatosis, Familial Cystic
|
|
|
| Autoimmune Polyendocrine Syndrome Type 1 |
|
Whitaker Syndrome
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
|
|
Autoimmune Polyglandular Syndrome I
|
Polyglandular Type I Autoimmune Syndrome
|
|
|
| Basal Ganglia Disease |
|
Basal Ganglia Diseases
|
Basal Ganglia Disorders
|
|
Abnormality Of The Basal Ganglia
|
|
|
| Gitelman Syndrome |
|
Familial Hypokalemia-Hypomagnesemia
|
Hypomagnesemia-Hypokalemia, Primary Renotubular, With Hypocalciuria
|
|
Potassium And Magnesium Depletion
|
GTLMNS
|
|
Gitelman'S Syndrome
|
Gs
|
|
Hypokalemia-Hypomagnesemia, Primary Renotubular, With Hypocalciuria
|
Tubular Hypomagnesemia-Hypokalemia With Hypocalcuria
|
|
Bartter Syndrome Gitelman Variant
|
Bartter Syndrome Hypocalciuric Variant
|
|
Primary Renotubular Hypomagnesemia-Hypokalemia With Hypocalciuria
|
|
|
| Diabetes Insipidus |
|
|
| Inflammatory Diarrhea |
|
|
| Epilepsy, Idiopathic Generalized 8 |
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 8
|
EIG8
|
|
Epilepsy Idiopathic Generalized, Susceptibility To, 8
|
Epilepsy Idiopathic Generalized 8
|
|
Idiopathic Generalized Epilepsy 8
|
Susceptibility To Idiopathic Generalized Epilepsy 8
|
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 8
|
|
|
| Hyperphosphatemia |
|
|
| Bartter Syndrome, Type 3 |
|
Bartter Disease Type 3
|
BARTS3
|
|
Bartter Syndrome Type 3
|
Bartter Syndrome, Classic
|
|
Classic Bartter Syndrome
|
Bartter Syndrome Classic
|
|
Bartter Syndrome Type Iii
|
Bartter Syndrome 3
|
|
|
| Rickets |
|
Vitamin D Deficiency
|
Active Rickets
|
|
Hypovitaminosis D
|
Nutritional Rickets
|
|
Vitamin D Deficiency Disease
|
Vitamin-D Deficiency Rickets
|
|
Vitamin D
|
Vitamin D-Dependent Rickets
|
|
Avitaminosis D
|
Infantile Osteomalacia
|
|
Juvenile Osteomalacia
|
|
|
| Uremia |
|
|
| 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
|
|
|
| Parathyroid Carcinoma |
|
Parathyroid Cancer
|
Parathyroid Neoplasms
|
|
Malignant Tumor Of Parathyroid Gland
|
PRTC
|
|
Carcinoma Of Parathyroid Gland
|
Malignant Neoplasm Of Parathyroid Gland
|
|
Parathyroid Gland Adenocarcinoma
|
Parathyroid Gland Cancer
|
|
Parathyroid Neoplasm
|
Parathyroid Gland Carcinoma
|
|
Malignant Neoplasm Of The Parathyroid
|
Neoplasm Of Parathyroid Gland
|
|
Parathyroid Gland Neoplasm
|
Cancer Of The Parathyroid
|
|
Cancer Of The Parathyroid Gland
|
Malignant Neoplasm Of Parathyroid
|
|
Malignant Parathyroid Gland Neoplasm
|
Malignant Parathyroid Gland Tumor
|
|
Malignant Parathyroid Neoplasm
|
Malignant Parathyroid Tumor
|
|
Malignant Tumor Of Parathyroid
|
Parathyroid Adenocarcinoma
|
|
Neoplasm Of The Parathyroid Gland
|
Carcinoma, Parathyroid
|
|
|
| Hypocalciuric Hypercalcemia, Familial, Type Ii |
|
HHC2
|
Familial Hypocalciuric Hypercalcemia 2
|
|
Fbh2
|
Familial Hypocalciuric Hypercalcemia Type 2
|
|
Hypocalciuric Hypercalcemia, Type Ii
|
Fhh Type 2
|
|
Familial Benign Hypercalcemia, Type Ii
|
Hypercalcemia, Familial Benign, Type Ii
|
|
Hypocalciuric Hypercalcemia Type Ii
|
Familial Benign Hypercalcemia, Type 2
|
|
Hypercalcemia, Familial Benign Type 2
|
Hypocalciuric Hypercalcemia, Familial, Type 2
|
|
Hypocalciuric Hypercalcemia, Familial 2
|
Familial Benign Hypercalcemia Type Ii
|
|
Hypocalciuric Hypercalcemia-2
|
|
|
| Primary Hyperparathyroidism |
|
Familial Primary Hyperparathyroidism
|
Hyperparathyroidism, Primary
|
|
Hyperparathyroidism Primary
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
Familial Benign Hypercalcemia
|
Familial Hyperparathyroidism
|
|
Parathyroid Enlargement
|
|
|
| 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
|
|
|
| Osteitis Fibrosa |
|
Osteitis Fibrosa Cystica
|
Hyperparathyroid Bone Disease
|
|
Osteitis Fibrosa Cystica Generalisata
|
Von Recklinghausen'S Bone Disease
|
|
Osteitis Fibrosa Disseminata
|
|
|
| Calciphylaxis |
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy, Hypertrophic, Familial
|
Familial Hypertrophic Cardiomyopathy
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Idiopathic Myocardial Hypertrophy
|
|
Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Cardiomyopathy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
|
Muscular Subaortic Stenosis
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
| Kenny-Caffey Syndrome |
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Basal Ganglia Calcification |
|
Fahr'S Syndrome
|
Fahr'S Disease
|
|
Fahr Disease
|
|
|
| Sialolithiasis |
|
Sialolith
|
Stone Of Salivary Gland Or Duct
|
|
Salivary Gland Calculi
|
Salivary Gland Stone
|
|
Calculus Of Salivary Gland Or Duct
|
Calculus Of Salivary Gland
|
|
Salivary Calculus
|
Salivary Gland Calculus
|
|
Salivary Stone
|
Salivary Duct Calculi
|
|
Sialodocholithiasis
|
|
|
| Hypoparathyroidism-Deafness-Renal Disease Syndrome |
|
Barakat Syndrome
|
Hypoparathyroidism, Deafness, Renal Disease Syndrome
|
|
Hdr Syndrome
|
Hypoparathyroidism, Sensorineural Deafness, And Renal Disease
|
|
|
| Autoimmune Polyendocrine Syndrome |
|
Autoimmune Polyendocrinopathy
|
Autoimmune Polyglandular Failure
|
|
Autoimmune Polyglandular Syndrome
|
Polyendocrinopathies, Autoimmune
|
|
Lloyd'S Syndrome
|
Aps
|
|
Polyendocrinopathies Autoimmune
|
Polyendocrine Autoimmunity Syndrome
|
|
Lloyd Syndrome
|
Polyglandular Autoimmune Deficiency
|
|
Progressive Pluriglandular Insufficiency
|
Pluriglandular Autoimmune Atrophy
|
|
Pluriglandular Autoimmune Syndrome
|
Thyroid-Adrenocortical Insufficiency Syndrome
|
|
|
| Diarrhea 1, Secretory Chloride, Congenital |
|
DIAR1
|
Chloride Diarrhea, Congenital, Finnish Type
|
|
Congenital Secretory Chloride Diarrhea 1
|
Congenital Chloride Diarrhea Finnish Type
|
|
Congenital Chloride Diarrhea
|
Chloridorrhea, Congenital
|
|
Congenital Chloride Diarrhoea Finnish Type
|
Congenital Chloridorrhea
|
|
Congenital Secretory Chloride Diarrhoea 1
|
Chloridorrhea Congenital
|
|
Cld
|
Diarrhea 1 Secretory Chloride Congenital
|
|
Diarrhea, Type 1, Chloride, Secretory, Congenital
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Bartter Syndrome, Type 2, Antenatal |
|
Bartter Disease Type 2
|
BARTS2
|
|
Hyperprostaglandin E Syndrome 2
|
Bartter Syndrome, Type 2
|
|
Bartter Syndrome Type 2
|
Hypokalemic Alkalosis With Hypercalciuria Antenatal 2
|
|
Hypokalemic Alkalosis With Hypercalciuria 2, Antenatal
|
Bartter Syndrome Type 2 Antenatal
|
|
Hypokalemic Alkalosis With Hypercalciuria 2 Antenatal
|
Bartter Syndrome Antenatal Type 2
|
|
Bartter Syndrome Type Ii
|
Bartter Syndrome 2, Antenatal
|
|
Abs2
|
Antenatal Bartter Syndrome 2
|
|
Bartter Syndrome 2
|
Bs2
|
|
Hyperprostanglandin E Syndrome 2
|
Bartter Syndrome, Antenatal , Type 2
|
|
Antley-Bixler Syndrome, Autosomal Dominant
|
|
|
| Hypocalciuric Hypercalcemia, Familial, Type I |
|
HHC1
|
Familial Hypocalciuric Hypercalcemia 1
|
|
Fhh1
|
Familial Benign Hypercalcemia 1
|
|
Fbh1
|
Hypocalciuric Hypercalcemia, Type I
|
|
Fhh Type 1
|
Hhc
|
|
Fhh
|
Hypercalcemia, Familial Benign
|
|
Hypocalciuric Hypercalcemia Type I
|
Familial Hypocalciuric Hypercalcemia Type 1
|
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
Familial Hypocalciuric Hypercalcemia Type I
|
|
Familial Benign Hypercalcemia Type 1
|
Hypercalcemia, Familial Benign Type 1
|
|
Hypocalciuric Hypercalcemia, Familial 1
|
Familial Benign Hypocalciuric Hypercalcemia 1
|
|
Fbhh1
|
|
|
| Osteomalacia |
|
|
| Diabetes Mellitus |
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Hearing Loss Disorder
|
|
Hearing Loss, Sensorineural
|
Central Hearing Loss
|
|
High Frequency Deafness
|
High Frequency Hearing Loss
|
|
High-Frequency Hearing Loss
|
Perceptive Deafness
|
|
Perceptive Hearing Loss
|
Perceptive Hearing Loss Or Deafness
|
|
Sensorineural Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Adrenal Cortex Adenoma
|
Corticotroph Pituitary Adenoma
|
|
Cushing'S Disease
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
|
Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| Nephrolithiasis, Calcium Oxalate |
|
Kidney Stones
|
Calculus Of Kidney
|
|
Kidney Calculi
|
Nephrolithiasis
|
|
Renal Calculi
|
Calcium Oxalate Urolithiasis
|
|
CAON
|
Urolithiasis, Calcium Oxalate
|
|
Calcium Oxalate Nephrolithiasis
|
Kidney Stone
|
|
Nephrolith
|
Renal Calculus
|
|
Urinary Stones
|
Renal Stone
|
|
Calculus, Kidney
|
Calculus, Renal
|
|
Renal Lithiasis
|
Renal Stones
|
|
Urolithiasis
|
Renal Calculus Or Stone
|
|
Stone In Kidney
|
Nephritic Calculus
|
|
Multiple Kidney Calculi
|
Multiple Kidney Calculus
|
|
Nephrolithiasis Nos
|
Pelvic Nephrolithiasis
|
|
Pelviolithiasis
|
Pelvis Nephrolithiasis
|
|
|
| Multiple Endocrine Neoplasia, Type I |
|
Multiple Endocrine Neoplasia Type 1
|
MEN1
|
|
Wermer Syndrome
|
Multiple Endocrine Neoplasia 1
|
|
Multiple Endocrine Neoplasia, Type 1
|
Men I
|
|
Endocrine Adenomatosis, Multiple
|
Mea I
|
|
Men Type I
|
Wermer'S Syndrome
|
|
Men1 Syndrome
|
Multiple Endocrine Adenomatosis
|
|
Endocrine Adenomatosis Multiple
|
Men 1
|
|
Familial Multiple Endocrine Neoplasia Type I
|
Neoplasia, Endocrine, Multiple, Type 1
|
|
Multiple Endocrine Neoplasia
|
|
|
| Nephrocalcinosis |
|
Hypercalcemic Nephropathy
|
|
|
