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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Vitamin D-Resistant Rickets, X-Linked Vitamin D-Resistant Rickets, X-Linked Vitamin D Resistant Rickets, X Linked Hypophosphatemic Rickets, X-Linked Recessive Hypophosphatemic Rickets, X-Linked Recessive Hypophosphatemic Rickets, X Linked Recessive 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 Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X Linked Dominant

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 related to "Familial Hypophosphatemic Rickets".

Below are MeSH descriptors whose meaning is more specific than "Familial Hypophosphatemic Rickets".

publications

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