Disease #07107 (AMC5 (arthrogryposis multiplex congenita, type 5), OMIM:618947)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	AMC5
Name	arthrogryposis multiplex congenita, type 5
OMIM ID	618947
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TOR1A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-10-01 09:47:20 +02:00 (CEST)
Date last edited	N/A

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