Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Acute Liver Failure | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35172013 | alcohol use disorder | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:16404797 more ... | autism spectrum disorder | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35663546 | cerebral infarction | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:15534263 | Colorectal Neoplasms | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:16332725 | Esophageal Neoplasms | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:18500343 | esophagus squamous cell carcinoma | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22960999 | Genetic Predisposition to Disease | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:16404797 and PMID:17590986 | Laryngeal Neoplasms | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:18500343 | metabolic dysfunction-associated steatotic liver disease | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:29718361 | Mouth Neoplasms | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:18500343 | obesity | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:20882379 | Pharyngeal Neoplasms | | ISO | ADH1B (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:18500343 | |