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

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Official abbreviation	HFTC
Name	calcinosis, tumoral, hyperphosphatemic, familial (HFTC)
OMIM ID	211900
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	FGF23, GALNT3, KL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	N/A