Disease #02322 (CMT2B (Charcot-Marie-Tooth disease, type 2B (CMT-2B)), OMIM:600882)

Official abbreviation CMT2B
Name Charcot-Marie-Tooth disease, type 2B (CMT-2B)
OMIM ID 600882
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene RAB7A
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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00404061 - - - F yes Egypt - - - - - CMT2B 52-y man with progressive weakness and wasting of both upper and lower limbs. There were no skeletal deformities. nerve conduction velocity study showed axonal peripheral neuropathy LMNA LMNA 1 6 Sherifa Ahmed Hamed
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