Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | breast cancer | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant tumor of breast | ClinVar | PMID:25741868 and PMID:28492532 | breast carcinoma | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Breast carcinoma | ClinVar | PMID:25741868 | colon carcinoma | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Carcinoma of colon | ClinVar | PMID:11317354 more ... | colorectal cancer | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | endometrial cancer | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial cancer | ClinVar | PMID:12702580 more ... | endometrial carcinoma | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial carcinoma | ClinVar | PMID:12702580 more ... | Hereditary Neoplastic Syndromes | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16885347 more ... | Hereditary Neoplastic Syndromes | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11317354 more ... | Hereditary Neoplastic Syndromes | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11586295 more ... | Hereditary Neoplastic Syndromes | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11586295 more ... | Hereditary Neoplastic Syndromes | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary cancer | ClinVar | PMID:25741868 and PMID:28492532 | hereditary nonpolyposis colorectal cancer type 7 | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Colorectal cancer more ... | ClinVar | PMID:11317354 more ... | intellectual disability | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability and mild | ClinVar | | Leukoencephalopathies | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: CACH/VWM syndrome | ClinVar | PMID:25741868 | leukoencephalopathy with vanishing white matter | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leukoencephalopathy with vanishing white matter | ClinVar | PMID:25741868 | Lynch syndrome | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11586295 more ... | Lynch syndrome | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11586295 more ... | Lynch syndrome 1 | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lynch syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | ovarian cancer | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ovarian cancer | ClinVar | PMID:25741868 and PMID:28492532 | primary ovarian insufficiency | | ISO | MLH3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Premature ovarian failure | ClinVar | PMID:25741868 and PMID:28492532 | | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - CTD
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