has characteristic has characteristic skin neoplasm familial tumoral calcinosis inborn errors of metabolism congenital hereditary skin disorder familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome https://www.malacards.org/card/tumoral_calcinosis_hyperphosphatemic_familial_1 HFTC Orphanet:306661 HHS MONDO:0100251 GARD:0010879 MEDGEN:360297 tumoral calcinosis, hyperphosphatemic, familial, 1 hyperphosphatemic familial tumoral calcinosis DOID:0111063 UMLS:C1876187 hypercalcemic tumoral calcinosis NCIT:C131851 familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome