MeSH Treeview
Query OMIM entry list
607364
-
BARTTER SYNDROME, TYPE 3
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Joint Diseases
Arthritis
Chondrocalcinosis
Gout
Rheumatic Diseases
Gout
Eye Diseases
Scleral Diseases
Uveal Diseases
Choroid Diseases
Male Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Adrenogenital Syndrome
Adrenal Hyperplasia, Congenital
Urologic Diseases
Kidney Diseases
Nephritis
Renal Tubular Transport, Inborn Errors
Bartter Syndrome
Hypophosphatemia, Familial
Pseudohypoaldosteronism
Urolithiasis
Urinary Calculi
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Adrenogenital Syndrome
Adrenal Hyperplasia, Congenital
Urologic Diseases
Kidney Diseases
Nephritis
Renal Tubular Transport, Inborn Errors
Bartter Syndrome
Hypophosphatemia, Familial
Pseudohypoaldosteronism
Urolithiasis
Urinary Calculi
Cardiovascular Diseases
Vascular Diseases
Hypertension
Hemic and Lymphatic Diseases
Hematologic Diseases
Polycythemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Urogenital Abnormalities
Disorders of Sex Development
Adrenogenital Syndrome
Adrenal Hyperplasia, Congenital
Genetic Diseases, Inborn
Adrenal Hyperplasia, Congenital
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Purine-Pyrimidine Metabolism, Inborn Errors
Gout
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Pseudohypoaldosteronism
Steroid Metabolism, Inborn Errors
Adrenal Hyperplasia, Congenital
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Alkalosis
Calcium Metabolism Disorders
Calcinosis
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Purine-Pyrimidine Metabolism, Inborn Errors
Gout
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Pseudohypoaldosteronism
Steroid Metabolism, Inborn Errors
Adrenal Hyperplasia, Congenital
Phosphorus Metabolism Disorders
Hypophosphatemia
Hypophosphatemia, Familial
Water-Electrolyte Imbalance
Hyperkalemia
Hypokalemia
Endocrine System Diseases
Adrenal Gland Diseases
Adrenal Hyperplasia, Congenital
Adrenocortical Hyperfunction
Hyperaldosteronism
Bartter Syndrome
Gonadal Disorders
Disorders of Sex Development
Adrenogenital Syndrome
Adrenal Hyperplasia, Congenital
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Calculi
Urinary Calculi
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Acute Disease
Growth Disorders
Hyperplasia
Signs and Symptoms
Body Weight
Signs and Symptoms, Digestive
Vomiting
Database Center for Life Science