Familial renal glucosuria
- Synonyms
- Familial renal glycosuria; RENAL GLUCOSURIA, AUTOSOMAL DOMINANT
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Autosomal dominant inheritance (Orphanet)
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (10 available)
Genes See tests for all associated and related genes
Also known as: SGLT2, SLC5A2
Summary: solute carrier family 5 member 2
Clinical features
Help- Abnormality of the genitourinary system
- Glycosuria
Glycosuria
- MedGen UID: 42267
- Concept ID: C0017979
- Finding: Finding
Abnormality of the genitourinary system
- Nocturnal enuresis
Nocturnal enuresis
- MedGen UID: 124355
- Concept ID: C0270327
- Finding: Mental or Behavioral Dysfunction
Abnormality of the genitourinary system
- Polyuria
Polyuria
- MedGen UID: 19404
- Concept ID: C0032617
- Finding: Sign or Symptom
Abnormality of the genitourinary system
- Glycosuria
- Abnormality of the nervous system
- Polydipsia
Polydipsia
- MedGen UID: 43214
- Concept ID: C0085602
- Finding: Sign or Symptom
Abnormality of the nervous system
- Polyphagia
Polyphagia
- MedGen UID: 9369
- Concept ID: C0020505
- Finding: Finding
Abnormality of the nervous system
- Polydipsia
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.