Familial Hypophosphatemic Rickets
"Familial Hypophosphatemic Rickets" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.
| Descriptor ID |
D053098
|
| MeSH Number(s) |
C05.116.198.816.875.500 C12.777.419.815.647.500 C13.351.968.419.815.647.500 C16.320.565.618.544.500 C16.320.565.861.647.500 C18.452.104.816.875.500 C18.452.174.845.875.500 C18.452.648.618.544.500 C18.452.648.861.647.500 C18.452.750.400.500.500 C18.452.750.400.750.500 C18.654.521.500.133.770.734.875.500
|
| Concept/Terms |
Familial Hypophosphatemic Rickets- Familial Hypophosphatemic Rickets
- Hypophosphatemic Rickets, Familial
- Rickets, Familial Hypophosphatemic
- Hypocalcemic Vitamin D-Resistant Rickets
- Hypocalcemic Vitamin D Resistant Rickets
- Rickets, Hereditary Vitamin D-Resistant
- Rickets, Hereditary Vitamin D Resistant
- Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol
- Vitamin D Resistant Rickets With End Organ Unresponsiveness To 1,25 Dihydroxycholecalciferol
- Vitamin D Resistant Rickets
- Vitamin D-Resistant Rickets, Hereditary
- Vitamin D Resistant Rickets, Hereditary
- Hereditary Vitamin D-Resistant Rickets
- Hereditary Vitamin D Resistant Rickets
- Hereditary Hypophosphatemic Rickets
- Hypophosphatemic Rickets, Hereditary
- Rickets, Hereditary Hypophosphatemic
- Generalized Resistance To 1,25-Dihydroxyvitamin D
- Generalized Resistance To 1,25 Dihydroxyvitamin D
Rickets, X-Linked Hypophosphatemic- Rickets, X-Linked Hypophosphatemic
- Hypophosphatemic Rickets, X-Linked
- X-Linked Hypophosphatemic Rickets
- Hypophosphatemia, X-Linked
- Hypophosphatemia, X Linked
- X-Linked Hypophosphatemia
- X Linked Hypophosphatemia
|
Below are MeSH descriptors whose meaning is more general than "Familial Hypophosphatemic Rickets".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Metabolic [C05.116.198]
- Rickets [C05.116.198.816]
- Rickets, Hypophosphatemic [C05.116.198.816.875]
- Familial Hypophosphatemic Rickets [C05.116.198.816.875.500]
- Male Urogenital Diseases [C12]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Renal Tubular Transport, Inborn Errors [C12.777.419.815]
- Hypophosphatemia, Familial [C12.777.419.815.647]
- Familial Hypophosphatemic Rickets [C12.777.419.815.647.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Renal Tubular Transport, Inborn Errors [C13.351.968.419.815]
- Hypophosphatemia, Familial [C13.351.968.419.815.647]
- Familial Hypophosphatemic Rickets [C13.351.968.419.815.647.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Metal Metabolism, Inborn Errors [C16.320.565.618]
- Hypophosphatemia, Familial [C16.320.565.618.544]
- Familial Hypophosphatemic Rickets [C16.320.565.618.544.500]
- Renal Tubular Transport, Inborn Errors [C16.320.565.861]
- Hypophosphatemia, Familial [C16.320.565.861.647]
- Familial Hypophosphatemic Rickets [C16.320.565.861.647.500]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Bone Diseases, Metabolic [C18.452.104]
- Rickets [C18.452.104.816]
- Rickets, Hypophosphatemic [C18.452.104.816.875]
- Familial Hypophosphatemic Rickets [C18.452.104.816.875.500]
- Calcium Metabolism Disorders [C18.452.174]
- Rickets [C18.452.174.845]
- Rickets, Hypophosphatemic [C18.452.174.845.875]
- Familial Hypophosphatemic Rickets [C18.452.174.845.875.500]
- Metabolism, Inborn Errors [C18.452.648]
- Metal Metabolism, Inborn Errors [C18.452.648.618]
- Hypophosphatemia, Familial [C18.452.648.618.544]
- Familial Hypophosphatemic Rickets [C18.452.648.618.544.500]
- Renal Tubular Transport, Inborn Errors [C18.452.648.861]
- Hypophosphatemia, Familial [C18.452.648.861.647]
- Familial Hypophosphatemic Rickets [C18.452.648.861.647.500]
- Phosphorus Metabolism Disorders [C18.452.750]
- Hypophosphatemia [C18.452.750.400]
- Hypophosphatemia, Familial [C18.452.750.400.500]
- Familial Hypophosphatemic Rickets [C18.452.750.400.500.500]
- Rickets, Hypophosphatemic [C18.452.750.400.750]
- Familial Hypophosphatemic Rickets [C18.452.750.400.750.500]
- Nutrition Disorders [C18.654]
- Malnutrition [C18.654.521]
- Deficiency Diseases [C18.654.521.500]
- Avitaminosis [C18.654.521.500.133]
- Vitamin D Deficiency [C18.654.521.500.133.770]
- Rickets [C18.654.521.500.133.770.734]
- Rickets, Hypophosphatemic [C18.654.521.500.133.770.734.875]
- Familial Hypophosphatemic Rickets [C18.654.521.500.133.770.734.875.500]
Below are MeSH descriptors whose meaning is more specific than "Familial Hypophosphatemic Rickets".
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