BIOMAT Database Logo BIOMAT Database Logo

Genetic heterogeneity of familial hypouricemia due to isolated renal tubular defect. 1981

T Suzuki, and K Kidoguchi, and A Hayashi

UI MeSH Term Description Entries
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D005799 Genes, Dominant Genes that influence the PHENOTYPE both in the homozygous and the heterozygous state. Conditions, Dominant Genetic,Dominant Genetic Conditions,Genetic Conditions, Dominant,Condition, Dominant Genetic,Dominant Gene,Dominant Genes,Dominant Genetic Condition,Gene, Dominant,Genetic Condition, Dominant
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D014527 Uric Acid An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN. 2,6,8-Trihydroxypurine,Ammonium Acid Urate,Monosodium Urate,Monosodium Urate Monohydrate,Potassium Urate,Sodium Acid Urate,Sodium Acid Urate Monohydrate,Sodium Urate,Sodium Urate Monohydrate,Trioxopurine,Urate,Acid Urate, Ammonium,Acid Urate, Sodium,Acid, Uric,Monohydrate, Monosodium Urate,Monohydrate, Sodium Urate,Urate Monohydrate, Monosodium,Urate Monohydrate, Sodium,Urate, Ammonium Acid,Urate, Monosodium,Urate, Potassium,Urate, Sodium,Urate, Sodium Acid
D015499 Renal Tubular Transport, Inborn Errors Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES. Kidney Tubular Transport, Inborn Errors,Kidney Tubular Transport, Inborn Error,Renal Tubular Transport Errors,Renal Tubular Transport, Inborn Error

Related Publications

T Suzuki, and K Kidoguchi, and A Hayashi
Familial renal hypouricemia due to isolated tubular defect.
January 1977, Advances in experimental medicine and biology,
T Suzuki, and K Kidoguchi, and A Hayashi
Inborn hypouricemia due to isolated renal tubular defect.
June 1979, Biomedicine / [publiee pour l'A.A.I.C.I.G.],
T Suzuki, and K Kidoguchi, and A Hayashi
Familial hypouricemia due to isolated renal tubular abnormality.
April 1978, Biomedicine / [publiee pour l'A.A.I.C.I.G.],
T Suzuki, and K Kidoguchi, and A Hayashi
Hypouricemia due to renal tubular defect.
June 1986, Archives of internal medicine,
T Suzuki, and K Kidoguchi, and A Hayashi
Hypouricemia due to an isolated defect in renal tubular urate reabsorption.
January 1980, Clinical nephrology,
T Suzuki, and K Kidoguchi, and A Hayashi
Inborn hypouricemia due to isolated defect in renal tubular uric acid transport.
April 1981, Israel journal of medical sciences,
T Suzuki, and K Kidoguchi, and A Hayashi
Hypouricemia due to isolated renal tubular defect. Dalmatian dog mutation in man.
September 1972, The American journal of medicine,
T Suzuki, and K Kidoguchi, and A Hayashi
Familial hypouricemia due to isolated renal tubular defect. Attenuated response of uric acid clearance to probenecid and pyrazinamide.
January 1977, Nephron,
T Suzuki, and K Kidoguchi, and A Hayashi
Hereditary renal hypouricemia. Isolated tubular defect of urate reabsorption.
May 1980, The Journal of pediatrics,
T Suzuki, and K Kidoguchi, and A Hayashi
Renal hypouricemia due to an isolated renal defect of urate transport.
January 1988, Nephron,
Copied contents to your clipboard!