Disease #02780 (CMT2L (Charcot-Marie-Tooth disease, type 2L (CMT-2L)), OMIM:608673)

Official abbreviation CMT2L
Name Charcot-Marie-Tooth disease, type 2L (CMT-2L)
OMIM ID 608673
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 HSPB8
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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00056468 - PubMed: Tang 2004, PubMed: Tang 2005 6-generation family, 26 affecteds (15F, 11M) F;M no China - - - - - CMT2L Charcot-Marie-Tooth disease 2L; see paper ... HSPB8 HSPB8 1 26 Johan den Dunnen
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