Disease #07106 (AMC6 (arthrogryposis multiplex congenita, type 6), OMIM:619334)

Global Variome shared LOVD

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

	Curator: Insa Buers

Official abbreviation	AMC6
Name	arthrogryposis multiplex congenita, type 6
OMIM ID	619334
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NEB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-10-01 09:41:10 +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.