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Hypophosphatemic Rickets
Hypophosphatemic rickets
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Diseases and disorders
(37)
X-linked hypophosphatemic rickets
Rickets
Cystine storage disease
Osteomalacia
Hypophosphatemia, familial
Hypophosphatemia, familial
Oncogenic osteomalacia
Phosphate diabetes
Glutaricaciduria
Hypercalcemia
Craniofrontonasal dysplasia
Floating harbor syndrome
Blepharophimosis ptosis epicanthus inversus
Hypophosphatasia
Hereditary motor sensory neuropathy
Craniotabes
VATER syndrome
Precocious puberty
Hypercalciuria
Polyostotic fibrous dysplasia
Hyperprolinemia
Hypocalcemia
Lysinuric protein intolerance
Lowe syndrome
Aminoaciduria
Nephrocalcinosis
Dwarfism
Chromosomal disorders
Renal osteodystrophy
Bowed legs
Hypoparathyroidism
Inborn error of metabolism
Urinary system
Chronic kidney disease
Hermansky-Pudlak syndrome
Homocystinuria
Metabolic Bone Disease
Tetanus
more...
Vitamin D
(29)
1,25-dihyd- roxyvitamin D3
Calcitriol
Hypervitaminosis D
Vitamin D3
Vitamin d deficiency
Vitamin d deficiency
22-Dihydro- ergocalciferol
7-Dehydroc- holesterol
7-Dehydrositosterol
Breast cancer; calcium and vitamin D
Calcifediol
Calcipotriol
Calcitriol receptor
Calcitroic acid
Cathelicidin
Dihydrotachysterol
Ergocalciferol
Ergosterol
GC (gene)
Lumisterol
Osteomalacia
Paricalcitol
Previtamin D3
Rickets
Tacalcitol
Tuberculosis treatment
Vitamin D and influenza
Vitamin D-dependent calcium-binding protein
Vitamin D5
X-linked hypophosphatemic rickets
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Skeletal disorders
Autosomal dominant hypophosphatemic rickets
Tumor induced osteomalacia
Rickets
Osteomalacia
Pediatrics
Rickets
Osteomalacia
Precocious puberty
Inborn error of metabolism
Autosomal recessive disorders
Cystine storage disease
Hyperprolinemia
Lysinuric protein intolerance
Hermansky-Pudlak syndrome
Homocystinuria
Genetic disorders
(13)
Inherited diseases
XLH
X-linked dominant
Cystine storage disease
Glutaricaciduria
Glutaricaciduria
Hypophosphatasia
Hereditary motor sensory neuropathy
VATER syndrome
Hyperprolinemia
Lysinuric protein intolerance
Chromosomal disorders
Hermansky-Pudlak syndrome
Homocystinuria
more...
Electrolyte disturbances
(35)
Hyperphosphatemia
Anion gap
Artificial tears
Bicarbonate buffering system
Central pontine myelinosis
Central pontine myelinosis
Cerebral salt-wasting syndrome
Contraction alkalosis
Darrow Yannet diagram
Dehydration
Fluid balance
Heat cramps
Hydrational fluids
Hyperbicarbonatemia
Hypercalcemia
Hyperchloremia
Hyperchloremic acidosis
Hyperkalemia
Hypermagnesemia
Hypernatremia
Hypobicarbonatemia
Hypocalcemia
Hypochloremia
Hypokalemia
Hypomagnesemia
Hyponatremia
Hypophosphatemia, familial
Hypotonic hyponatremia
Isotonic hyponatremia
Keratoconj- unctivitis sicca
Milk-alkali syndrome
Milk-and-alkali tetany
Rehydration
Serum osmotic gap
Water intoxication
Water-electrolyte imbalance
more...
Genetics
X linked
X-linked recessive
Mutations
Chromosomes
Genetic disorders
Inherited diseases
Parathyroid disorders
Hyperparathyroidism
Secondary hyperparathyroidism
Hypoparathyroidism
Parathyroid disease
Parathyroid gland
Tertiary hyperparathyroidism
Symptoms
Photophobia
Hypertrophy
Bone pain
Short stature
Bowed legs
See also
(20)
PHEX gene
FGF23
Cystinosin
SLC34A3
Cystine
Cystine
Fanconi syndrome
Reabsorption
J. Pediatr. Endocrinol. Metab.
Sodium/phosphate cotransporter
University of California at San Diego School of Medicine
Autosomal recessive
Parathyroid hormone
Short stature
MEPE
Renal
Lignac
Cysteamine
Alkaline phosphatase
Renal transplantation
Heterozygous
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