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

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

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	-
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	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.