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MIM:118700 - CHOREA, BENIGN HEREDITARY; BHC
Xenbase Genes: nkx2-1
Human Disease Resource: MIM
| MONDO:0008979 - chorea, benign familial |
| MONDO:0021011 - hereditary progressive chorea without dementia |
| DOID:12859 - choreatic disease |
|
| MONDO:0008979 - chorea, benign familial |
| MONDO:0021011 - hereditary progressive chorea without dementia |
| DOID:12859 - choreatic disease |