Disease #06720 (AMC3 (arthrogryposis multiplex congenita, type 3, myogenic), OMIM:618484)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	AMC3
Name	arthrogryposis multiplex congenita, type 3, myogenic
OMIM ID	618484
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SYNE1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2024-10-01 09:44:24 +02:00 (CEST)

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