Disease #02356 (CMT4B1 (Charcot-Marie-Tooth disease, type 4B1 (CMT-4B1)), OMIM:601382)

Official abbreviation CMT4B1
Name Charcot-Marie-Tooth disease, type 4B1 (CMT-4B1)
OMIM ID 601382
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MTMR2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00398752 580 PubMed: Ferese 2021 2-generation family, 2 affected, 2 unaffected carrier parents F - Italy - >30y - - - CMT4B1 Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) MTMR2 MTMR2 1 1 Yvet den Hartog
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