Disease #01245 (CMT1B (Charcot-Marie-Tooth disease, type IB (CMT-1B)), OMIM:118200)
Official abbreviation |
CMT1B |
Name |
Charcot-Marie-Tooth disease, type IB (CMT-1B) |
OMIM ID |
118200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
44 |
Phenotype entries for this disease |
44 |
Associated with 1 gene |
MPZ |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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