All diseases

OMIM ID
211900
OMIM term:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL; HFTC
Alternative terms:
CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIA
TUMORAL CALCINOSIS, PRIMARY HYPERPHOSPHATEMIC; PHPTC
LIPOCALCINOGRANULOMATOSIS
TEUTSCHLAENDER DISEASE, FAMILIAL
MORBUS TEUTSCHLAENDER
HYPEROSTOSIS-HYPERPHOSPHATEMIA SYNDROME; HHS
HYPEROSTOSIS WITH HYPERPHOSPHATEMIA
CORTICAL HYPEROSTOSIS WITH HYPERPHOSPHATEMIA
(∗) Location:
12p13.32   13q13.1   2q24.3  
(†) Associated OMIM genes:
FGF23   GALNT3   KL  
(‡) Associated MGI genes:
Galnt3  

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* quick link - http://q.sanger.ac.uk/092y73xq