MeSH Browser

MeSH Heading: Renal Tubular Transport, Inborn Errors
Tree Number(s): C12.050.351.968.419.815; C12.200.777.419.815; C12.950.419.815; C16.320.565.893; C16.320.831; C18.452.648.893
Unique ID: D015499
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D015499
Annotation: general or unspecified; prefer specifics; coordinate with specific metabolite /‌metab
Scope Note: Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.
Entry Version: RENAL TUB TRANSP INBORN ERR
Entry Term(s): Kidney Tubular Transport, Inborn Error; Kidney Tubular Transport, Inborn Errors; Renal Tubular Transport Errors; Renal Tubular Transport, Inborn Error
NLM Classification #: WJ 301
Public MeSH Note: 65
History Note: 65
Date Established: 1965/01/01
Date of Entry: 1964/07/01
Revision Date: 2021/06/30

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Urogenital Diseases [C12]
- Female Urogenital Diseases and Pregnancy Complications [C12.050]
  - Female Urogenital Diseases [C12.050.351]
    - Urologic Diseases [C12.050.351.968]
      - Kidney Diseases [C12.050.351.968.419]
        
        AIDS-Associated Nephropathy [C12.050.351.968.419.050]
        
        Anuria [C12.050.351.968.419.078]
        
        Diabetes Insipidus [C12.050.351.968.419.135]
        
        Diabetic Nephropathies [C12.050.351.968.419.192]
        
        Hepatorenal Syndrome [C12.050.351.968.419.291]
        
        Hydronephrosis [C12.050.351.968.419.307]
        
        Hyperoxaluria [C12.050.351.968.419.313]
        
        Hypertension, Renal [C12.050.351.968.419.331]
        
        Kidney Cortex Necrosis [C12.050.351.968.419.393]
        
        Kidney Diseases, Cystic [C12.050.351.968.419.403]
        
        Kidney Neoplasms [C12.050.351.968.419.473]
        
        Kidney Papillary Necrosis [C12.050.351.968.419.493]
        
        Nephritis [C12.050.351.968.419.570]
        
        Nephrocalcinosis [C12.050.351.968.419.590]
        
        Nephrolithiasis [C12.050.351.968.419.600]
        
        Nephrosclerosis [C12.050.351.968.419.610]
        
        Nephrosis [C12.050.351.968.419.630]
        
        Perinephritis [C12.050.351.968.419.685]
        
        Renal Artery Obstruction [C12.050.351.968.419.775]
        
        Renal Insufficiency [C12.050.351.968.419.780]
        
        Renal Nutcracker Syndrome [C12.050.351.968.419.787]
        
        Chronic Kidney Disease-Mineral and Bone Disorder [C12.050.351.968.419.795]
        
        Renal Tubular Transport, Inborn Errors [C12.050.351.968.419.815]
        
        Acidosis, Renal Tubular [C12.050.351.968.419.815.093]
        
        Bartter Syndrome [C12.050.351.968.419.815.279]
        
        Dent Disease [C12.050.351.968.419.815.364]
        
        Fanconi Syndrome [C12.050.351.968.419.815.450]
        
        Gitelman Syndrome [C12.050.351.968.419.815.491]
        
        Glycosuria, Renal [C12.050.351.968.419.815.532]
        
        Hypophosphatemia, Familial [C12.050.351.968.419.815.647]
        
        Liddle Syndrome [C12.050.351.968.419.815.683]
        
        Oculocerebrorenal Syndrome [C12.050.351.968.419.815.720]
        
        Pseudohypoaldosteronism [C12.050.351.968.419.815.770]
        
        Renal Aminoacidurias [C12.050.351.968.419.815.885]
        
        Tuberculosis, Renal [C12.050.351.968.419.912]
        
        Uremia [C12.050.351.968.419.936]
        
        Zellweger Syndrome [C12.050.351.968.419.978]

Urogenital Diseases [C12]
- Male Urogenital Diseases [C12.200]
  - Urologic Diseases [C12.200.777]
    - Kidney Diseases [C12.200.777.419]

Urogenital Diseases [C12]
- Urologic Diseases [C12.950]
  - Kidney Diseases [C12.950.419]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]

Renal Tubular Transport, Inborn Errors Preferred

Renal Tubular Transport, Inborn Errors MeSH Descriptor Data 2024