Disease #05791 (CMT2Z (Charcot-Marie-Tooth disease, type 2Z (CMT2Z)), OMIM:616688)
Official abbreviation |
CMT2Z |
Name |
Charcot-Marie-Tooth disease, type 2Z (CMT2Z) |
OMIM ID |
616688 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
MORC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-07-23 15:02:57 +02:00 (CEST) |
Date last edited |
N/A |
Individuals
|
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