Rickets
41hereditary hypophosphatemic rickets with hypercalciuria — a form of familial hypophosphatemic rickets caused by mutation in the SLC34A3 gene (locus: 9q34), which encodes a cotransporter important in maintenance of inorganic phosphate concentration at the kidney; hypophosphatemia is accompanied by… …
42vitamin D–dependent rickets type I — an autosomal recessive disorder characterized by rickets with myopathy, hypocalcemia, moderate hypophosphatemia, secondary hyperparathyroidism, and subnormal serum concentrations of 1,25 dihydroxyvitamin D. The disorder can be overcome by high… …
43adult rickets — osteomalacia …
44fetal rickets — achondroplasia …
45oncogenous rickets — oncogenous osteomalacia occurring in children …
46pseudodeficiency rickets — vitamin D–dependent r. type I and type II …
47pseudovitamin D–deficiency rickets — vitamin D–dependent r., type I; the term is sometimes used to denote types I and II collectively …
48refractory rickets — vitamin D–resistant r …
49scurvy rickets — rachitic changes in the skeleton associated with infantile scurvy …
50vitamin D–dependent rickets type II — an autosomal recessive disorder similar to type I but with elevated serum concentrations of 1,25 dihydroxyvitamin D. The disorder cannot be overcome by high levels of vitamin D or its metabolites and is caused by end organ refractoriness to the… …