Disease #06207 (AMCNACC (Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum), OMIM:618766)

Official abbreviation	AMCNACC
Name	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum
OMIM ID	618766
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCYL2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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

Global Variome shared LOVD