| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia | ALG9 | disease | C1849762 | Biomarker | 0.6 | disgenet |
| Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia | ALG9 | disease | C1849762 | CausalMutation | 0.6 | disgenet |
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