Disease #07014 (MARTS2 (Martsolf syndrome, type 2), OMIM:619420)

Global Variome shared LOVD

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

	Curator: Sarah Leigh

Official abbreviation	MARTS2
Name	Martsolf syndrome, type 2
OMIM ID	619420
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAB3GAP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-07-24 14:23:42 +02:00 (CEST)
Date last edited	N/A

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