Disease #05846 (KPTS (Keipert syndrome (KPTS)), OMIM:301026)

Global Variome shared LOVD

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

Official abbreviation	KPTS
Name	Keipert syndrome (KPTS)
OMIM ID	301026
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GPC4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-29 14:48:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.