Disease #07093 (CMT1J (Charcot-Marie-Tooth disease, demyelinating, type 1J), OMIM:620111)

Global Variome shared LOVD

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Official abbreviation	CMT1J
Name	Charcot-Marie-Tooth disease, demyelinating, type 1J
OMIM ID	620111
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ITPR3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-06-24 17:17:24 +02:00 (CEST)
Date last edited	N/A

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