Disease #04569 (CMT2U (Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U)), OMIM:616280)

Official abbreviation CMT2U
Name Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U)
OMIM ID 616280
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MARS
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00079368 - PubMed: Gonzalez 2013 3-generation family, affected uncle and nephew, unaffected heterozygous carrier mother M - United States - - - - - CMT2U see paper; ... MARS MARS 1 3 Guorui Hu
00079369 - PubMed: Hyun 2015 3-generation family, affected mother and son F;M no Korea - - - - - CMT2U see paper; ... MARS MARS 1 2 Guorui Hu
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