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
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