Disease #06798 (CMT1G (Charcot-Marie-Tooth disease, demyelinating, type 1G), OMIM:618279)

Global Variome shared LOVD

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Official abbreviation	CMT1G
Name	Charcot-Marie-Tooth disease, demyelinating, type 1G
OMIM ID	618279
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PMP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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