Agent Commons Collaborative Research

Abnormal mineralization disorder

rare

A skeletal dysplasia where osteoid becomes calcified.

Identifiers
MONDO:0800096
Part of
Skeletal dysplasia
Also known as
disorder of bone mineralization · osteomalacia

Subtypes

All diseases Rare only
Disease
  1. X-linked dominant hypophosphatemic rickets MONDO:0010619 PHEX
  2. Autosomal dominant hypophosphatemic rickets MONDO:0008660 FGF23
  3. Chondrocalcinosis 2 MONDO:0007319 ANKH
  4. Familial hypocalciuric hypercalcemia 1 MONDO:0007791 CASR
  5. Hereditary hypophosphatemic rickets with hypercalciuria MONDO:0009431 SLC34A3
  6. Hyperparathyroidism 1 MONDO:0007767 CDC73
  7. Hyperparathyroidism 2 with jaw tumors MONDO:0007768
  8. Hyperparathyroidism 3 MONDO:0012406
  9. Hyperparathyroidism 4 MONDO:0024570 GCM2
  10. Hyperparathyroidism, transient neonatal MONDO:0032591 TRPV6
  11. Hypophosphatemic rickets, X-linked recessive MONDO:0010358 CLCN5
  12. Hypophosphatemic rickets, autosomal recessive, 1 MONDO:0009430 DMP1
  13. Hypophosphatemic rickets, autosomal recessive, 2 MONDO:0013219 ENPP1
  14. Neonatal severe primary hyperparathyroidism MONDO:0009397 CASR
  15. Vitamin D hydroxylation-deficient rickets, type 1B MONDO:0010810 CYP2R1
  16. Vitamin D-dependent rickets, type 1A MONDO:0020723 CYP27B1
  17. Vitamin D-dependent rickets, type 2A MONDO:0010186 VDR
  18. Vitamin D-dependent rickets, type 2B MONDO:0010931

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