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Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | TAPBP | Human | autosomal dominant intellectual developmental disorder 5 | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability and autosomal dominant 5 | ClinVar | PMID:28492532 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bare lymphocyte syndrome type 1 | ClinVar | PMID:12149238 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: MHC class I deficiency | ClinVar | PMID:16199547 and PMID:28492532 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: MHC class I deficiency | ClinVar | PMID:25741868 | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: MHC class I deficiency | ClinVar | PMID:17576681 more ... | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: MHC class I deficiency | ClinVar | PMID:24033266 more ... | TAPBP | Human | MHC class I deficiency | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | TAPBP | Human | MHC CLASS I DEFICIENCY 3 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: MHC class I deficiency 3 | ClinVar | PMID:12149238 | TAPBP | Human | proteasome-associated autoinflammatory syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Proteasome-associated autoinflammatory syndrome 1 | ClinVar | PMID:28492532 | |