Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autistic disorder | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autism | ClinVar | PMID:21681106 and PMID:30208311 | chromosome 3q29 microdeletion syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chromosome 3q29 microdeletion syndrome | ClinVar | | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | Knobloch Syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Knobloch syndrome | ClinVar | PMID:14695535 more ... | Knobloch Syndrome Type II | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Knobloch syndrome 2 | ClinVar | PMID:25741868 | schizophrenia | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Schizophrenia | ClinVar | PMID:21681106 and PMID:30208311 | |