Disease #04472 (HFTC (calcinosis, tumoral, hyperphosphatemic, familial (HFTC)), OMIM:211900)

Official abbreviation HFTC
Name calcinosis, tumoral, hyperphosphatemic, familial (HFTC)
OMIM ID 211900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes FGF23, GALNT3, KL
Associated tissues -
Disease features -
Remarks -