MeSH Treeview
Query OMIM entry list
604144
SLC7A9
SOLUTE CARRIER FAMILY 7 (CATIONIC AMINO ACID TRANSPORTER, y+ SYSTEM), MEMBER 9
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephrolithiasis
Kidney Calculi
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Urolithiasis
Nephrolithiasis
Kidney Calculi
Urinary Calculi
Kidney Calculi
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephrolithiasis
Kidney Calculi
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Urolithiasis
Nephrolithiasis
Kidney Calculi
Urinary Calculi
Kidney Calculi
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Mitochondrial Diseases
Mitochondrial Myopathies
Endocrine System Diseases
Parathyroid Diseases
Hypoparathyroidism
Polyendocrinopathies, Autoimmune
Immune System Diseases
Autoimmune Diseases
Polyendocrinopathies, Autoimmune
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Calculi
Urinary Calculi
Kidney Calculi
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
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