Disease #01247 (CMT1A (Charcot-Marie-Tooth disease, type IA (CMT1A)), OMIM:118220)
Official abbreviation |
CMT1A |
Name |
Charcot-Marie-Tooth disease, type IA (CMT1A) |
OMIM ID |
118220 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PMP22 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-06-30 17:23:15 +02:00 (CEST) |
Individuals
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