Dataset | OMIM Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
External Link | http://www.omim.org/entry/614455 |
Similar Terms | |
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1 genes associated with the charcot-marie-tooth disease, dominant intermediate e phenotype from the curated OMIM Gene-Disease Associations dataset.
Symbol | Name |
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INF2 | inverted formin, FH2 and WH2 domain containing |