Often increased
0No markers in this group.
Everyone Healthy Library
Condition / disease reference page from the Everyone Healthy database.
Connected health information
Condition overview
No related signs or symptoms are listed yet.
Medication information is educational only. A doctor or pharmacist should advise whether any medicine is appropriate.
Grouped by treatment type. These are educational database links, not personal treatment recommendations. Evidence labels are shown only where stored in the EH database.
No linked treatment or supportive options are listed yet.
These are pulled from both EH diagnostic-test link tables, including the older large test-link table.
This visual map uses existing EH database links to show biological agents and lab markers reported as increased, decreased, or associated with this condition. These are educational relationships only; test results must be interpreted by a qualified clinician because ranges vary by lab, method, age, sex and clinical context.
No markers in this group.
No markers in this group.
Introduction / full article
Hypophosphatemic Rickets (Autosomal dominant hypophosphatemic rickets(ADHR)) is a rare hereditary disease in which excessive loss of phosphate in the urine leads to poorly formed bones (rickets), bone pain, and tooth abscesses. ADHR is caused by a mutation in the fibroblast growth factor 23 (FGF23). ADHR affects men and women equally; symptoms may become apparent at any point from childhood through early adulthood. Blood tests reveal low levels of phosphate (hypophosphatemia) and inappropriately normal levels of vitamin D. Treatment consists of increasing phosphate intake and high doses of vitamin D. Occasionally, hypophosphatemia may improve over time as urine losses of phosphate partially correct.