Disease #02709 (CMT2K (Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K), OMIM:607831)

Official abbreviation CMT2K
Name Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K
OMIM ID 607831
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 5
Associated with 2 genes GDAP1, JPH1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-09-26 08:42:49 +02:00 (CEST)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00103670 ? PubMed: Crimella 2010 - - - - - - - - - CMT2K Charcot-Marie-Tooth disease 2K, axonal GDAP1 GDAP1 1 1 Johan den Dunnen
00103696 ? PubMed: Crimella 2010 - - - - - - - - - CMT2K Charcot-Marie-Tooth disease 2K, axonal GDAP1 GDAP1 1 1 Johan den Dunnen
00103700 ? PubMed: Cassereau 2009 - - - - - - - - - CMT2K Charcot-Marie-Tooth disease 2K GDAP1 GDAP1 1 1 Johan den Dunnen
00103714 ? PubMed: Crimella 2010 - - - - - - - - - CMT2K Charcot-Marie-Tooth disease 2K, axonal GDAP1 GDAP1 1 1 Johan den Dunnen
00398625 1196 PubMed: Ferese 2021 2-generation family, 2 affected M - Italy - >69y - - - CMT2K see paper; ..., peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) GDAP1 GDAP1 1 1 Yvet den Hartog
00400223 Family 2 II-1 PubMed: Chen 2020 2-generation family, 1 affected, 2 unaffected carriers M - China - >05y - - - CMT2K - GDAP1 GDAP1 2 1 Yvet den Hartog
00400224 Family 3 II-2 PubMed: Chen 2020 3-generation family, 1 affected, 1 unaffected carrier, 1 unaffected, 2 untested F - China - >73y - - - CMT2K - GDAP1 GDAP1 1 1 Yvet den Hartog
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