Disease #02751 (CMTDIC (Charcot-Marie-Tooth disease, dominant intermediate, type C (CMTDIC)), OMIM:608323)

Official abbreviation CMTDIC
Name Charcot-Marie-Tooth disease, dominant intermediate, type C (CMTDIC)
OMIM ID 608323
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene YARS
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

4 entries on 1 page. Showing entries 1 - 4.
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00089189 - PubMed: Hyun 2015 3-generation family, affected male M no Korea - - - - - CMTDIC see paper; ... YARS YARS 1 1 Johan den Dunnen
00089192 - PubMed: Jordanova 2006 family - no United States - - - - - CMTDIC see paper; … YARS YARS 1 2 Johan den Dunnen
00089193 - PubMed: Jordanova 2006 2-generation family, 1 affected, unaffected non-carrier parents F no Belgium - - - - - CMTDIC see paper; … YARS YARS 1 1 Johan den Dunnen
00089194 - PubMed: Jordanova 2006 family - no Bulgaria - - - - - CMTDIC see paper; … YARS YARS 1 2 Johan den Dunnen
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