Disease #05889 (CMT2A2B (Charcot-Marie-Tooth disease, type 2A2B (CMT2A2B)), OMIM:617087)

Official abbreviation CMT2A2B
Name Charcot-Marie-Tooth disease, type 2A2B (CMT2A2B)
OMIM ID 617087
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MFN2
Associated tissues -
Disease features -
Remarks -
Date created 2021-01-12 13:05:55 +01:00 (CET)
Date last edited N/A

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