Disease #07037 (CMT1I (Charcot-Marie-Tooth disease, demyelinating, type 1I), OMIM:619742)

Global Variome shared LOVD

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Official abbreviation	CMT1I
Name	Charcot-Marie-Tooth disease, demyelinating, type 1I
OMIM ID	619742
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POLR3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-10-24 16:47:04 +02:00 (CEST)
Date last edited	N/A

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