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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