Hypophosphatemic Rickets, X-Linked Dominant
"Hypophosphatemic Rickets, X-Linked Dominant" 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.
An X-linked disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. This disorder is caused by mutations in PHEX PHOSPHATE REGULATING NEUTRAL ENDOPEPTIDASE.
| Descriptor ID |
D053098
|
| MeSH Number(s) |
C05.116.198.816.500 C12.777.419.815.647.500 C13.351.968.419.815.647.500 C16.320.322.239 C16.320.565.618.544.500 C16.320.565.861.647.500 C18.452.174.845.500 C18.452.648.618.544.500 C18.452.648.861.647.500 C18.654.521.500.133.770.734.500
|
| Concept/Terms |
Hypophosphatemic Rickets, X-Linked Dominant- Hypophosphatemic Rickets, X-Linked Dominant
- Hypophosphatemic Rickets, X Linked Dominant
- Vitamin D-Resistant Rickets, X-Linked
- Vitamin D Resistant Rickets, X Linked
- Hypophosphatemic Vitamin D-Resistant Rickets
- Hypophosphatemia, Vitamin D-Resistant Rickets
- Hypophosphatemia, X-Linked
- Hypophosphatemia, X Linked
- Rickets, Vitamin D-Resistant
- Rickets, Vitamin D Resistant
- Vitamin D-Resistant Rickets
- Rickets, X-Linked Hypophosphatemic
- Hypophosphatemic Rickets, X-Linked
- X-Linked Hypophosphatemic Rickets
- X-Linked Hypophosphatemia
- X Linked Hypophosphatemia
|
Below are MeSH descriptors whose meaning is more general than "Hypophosphatemic Rickets, X-Linked Dominant".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Metabolic [C05.116.198]
- Rickets [C05.116.198.816]
- Hypophosphatemic Rickets, X-Linked Dominant [C05.116.198.816.500]
- 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]
- Hypophosphatemic Rickets, X-Linked Dominant [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]
- Hypophosphatemic Rickets, X-Linked Dominant [C13.351.968.419.815.647.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Hypophosphatemic Rickets, X-Linked Dominant [C16.320.322.239]
- Metabolism, Inborn Errors [C16.320.565]
- Metal Metabolism, Inborn Errors [C16.320.565.618]
- Hypophosphatemia, Familial [C16.320.565.618.544]
- Hypophosphatemic Rickets, X-Linked Dominant [C16.320.565.618.544.500]
- Renal Tubular Transport, Inborn Errors [C16.320.565.861]
- Hypophosphatemia, Familial [C16.320.565.861.647]
- Hypophosphatemic Rickets, X-Linked Dominant [C16.320.565.861.647.500]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Calcium Metabolism Disorders [C18.452.174]
- Rickets [C18.452.174.845]
- Hypophosphatemic Rickets, X-Linked Dominant [C18.452.174.845.500]
- Metabolism, Inborn Errors [C18.452.648]
- Metal Metabolism, Inborn Errors [C18.452.648.618]
- Hypophosphatemia, Familial [C18.452.648.618.544]
- Hypophosphatemic Rickets, X-Linked Dominant [C18.452.648.618.544.500]
- Renal Tubular Transport, Inborn Errors [C18.452.648.861]
- Hypophosphatemia, Familial [C18.452.648.861.647]
- Hypophosphatemic Rickets, X-Linked Dominant [C18.452.648.861.647.500]
- 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]
- Hypophosphatemic Rickets, X-Linked Dominant [C18.654.521.500.133.770.734.500]
Below are MeSH descriptors whose meaning is more specific than "Hypophosphatemic Rickets, X-Linked Dominant".
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