Disease #00185 (CMT2A1 (CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1), OMIM:118210)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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	Curator: Florian Bayersdorfer

Official abbreviation	CMT2A1
Name	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1
OMIM ID	118210
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIF1B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-07-17 11:53:16 +00:00 (UTC)
Date last edited	N/A