. _:vb50944154 . . "A calcinosis characterized by autosomal recessive inheritance of elevated blood calcium levels and calcium phosphate crystals in cutaneous and subcutaneous tissues that has_material_basis_in mutation in the GALNT3 gene, the FGF23 gene, or the KL gene."^^ . "disease_ontology"^^ . "hyperphosphatemia hyperostosis"@en . "familial Teutschlaender disease"@en . "hyperphosphatemia hyperostosis syndrome"@en . _:vb50944154 . _:vb50944154 . . "familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome"@en . "morbus Teutschlaender"@en . "hyperphosphatemic familial tumoral calcinosis"^^ . "HHS"@en . "GARD:10879"^^ . "primary hyperphosphatemic tumoral calcinosis"@en . "ORDO:306661"^^ . "cortical hyperostosis with hyperphosphatemia"@en . . "DOID:0111063"^^ . "ICD10CM:M11.2"^^ . "hyperostosis with hyperphosphatemia"@en . "PHPTC"@en . "hypercalcemic tumoral calcinosis"@en . _:vb50944154 . "OMIM:211900"^^ . "lipocalcinogranulomatosis"@en . "tumoral calcinosis with hyperphosphatemia"@en . "hyperphosphatemia tumoral calcinosis"@en . _:vb50944154 . "HFTC"@en . .