Disorder characterized by hypophosphatemi, rickets, osteomalacia, resulting from lack of phosphate reabsorption by the kidneys and possible defects in vitamin D metabolism.
Examples for "acquired vitamin d resistant rickets"
1
X-linked hypophosphatemicrickets and autosomal dominant hypophosphatemicrickets are inherited phosphate wasting disorders.
2
Human DMP1 mutations are responsible for the condition known as autosomal recessive hypophosphatemicrickets.
3
A subset of those who survive eventually develop hypophosphatemicrickets.
4
Skeletal muscle dysfunction accompanies the clinical disorders of chronic kidney disease (CKD) and hereditary hypophosphatemicrickets.
5
X-linked hypophosphatemicrickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
1
X-linked hypophosphatemicrickets and autosomal dominant hypophosphatemicrickets are inherited phosphate wasting disorders.
2
Human DMP1 mutations are responsible for the condition known as autosomal recessive hypophosphatemicrickets.
3
A subset of those who survive eventually develop hypophosphatemicrickets.
4
Skeletal muscle dysfunction accompanies the clinical disorders of chronic kidney disease (CKD) and hereditary hypophosphatemicrickets.
5
X-linked hypophosphatemicrickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
6
X-linked hypophosphatemicrickets results from mutations in the PHEX gene, which codes for a protein that is a member of the neutral endopeptidase family.