- OMIM ID
-
239000
- OMIM term:
- PAGET DISEASE, JUVENILE
- Alternative terms:
-
JUVENILE PAGET DISEASE; JPD
HYPEROSTOSIS CORTICALIS DEFORMANS JUVENILIS
HYPERPHOSPHATASIA, FAMILIAL IDIOPATHIC
HYPERPHOSPHATASEMIA, CHRONIC CONGENITAL IDIOPATHIC
OSTEOECTASIA, FAMILIAL
- (∗) Location:
- 8q24.12
- (†) Associated OMIM genes:
- TNFRSF11B
- (‡) Associated MGI genes:
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