Disease #05889 (CMT2A2B (Charcot-Marie-Tooth disease, type 2A2B (CMT2A2B)), OMIM:617087)
Official abbreviation |
CMT2A2B |
Name |
Charcot-Marie-Tooth disease, type 2A2B (CMT2A2B) |
OMIM ID |
617087 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MFN2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-01-12 13:05:55 +01:00 (CET) |
Date last edited |
N/A |
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