Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | WDR19 | Pig | asphyxiating thoracic dystrophy | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | WDR19 | Pig | asphyxiating thoracic dystrophy | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jeune thoracic dystrophy | ClinVar | PMID:16199547 more ... | WDR19 | Pig | asphyxiating thoracic dystrophy | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | WDR19 | Pig | asphyxiating thoracic dystrophy 1 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chondroectodermal dysplasia-like syndrome | ClinVar | PMID:22019273 more ... | WDR19 | Pig | asphyxiating thoracic dystrophy 5 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | WDR19 | Pig | Bardet-Biedl syndrome | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bardet-Biedl syndrome | ClinVar | PMID:25741868 and PMID:28492532 | WDR19 | Pig | Beemer-Langer syndrome | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Type IV short rib polydactyly syndrome | ClinVar | PMID:16199547 more ... | WDR19 | Pig | cone dystrophy | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cone dystrophy | ClinVar | PMID:22019273 more ... | WDR19 | Pig | connective tissue disease | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | WDR19 | Pig | cranioectodermal dysplasia | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cranioectodermal dysplasia | ClinVar | PMID:22019273 more ... | WDR19 | Pig | cranioectodermal dysplasia 4 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cranioectodermal dysplasia 4 | ClinVar | PMID:17576681 more ... | WDR19 | Pig | Craniosynostosis Syndrome, Autosomal Recessive | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:25741868 more ... | WDR19 | Pig | fundus dystrophy | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:22019273 more ... | WDR19 | Pig | genetic disease | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:16199547 more ... | WDR19 | Pig | Hyperglycinemia, Lactic Acidosis, and Seizures | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: HYPERGLYCINEMIA more ... | ClinVar | PMID:28492532 | WDR19 | Pig | intellectual disability | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability | ClinVar | PMID:25741868 and PMID:28492532 | WDR19 | Pig | Leber congenital amaurosis | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leber congenital amaurosis | ClinVar | PMID:23559409 more ... | WDR19 | Pig | nephronophthisis 13 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nephronophthisis 13 | ClinVar | PMID:16199547 more ... | WDR19 | Pig | retinitis pigmentosa | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar | PMID:25741868 more ... | WDR19 | Pig | Senior-Loken syndrome | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | WDR19 | Pig | Senior-Loken Syndrome 8 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Senior-Loken syndrome 8 | ClinVar | PMID:16199547 more ... | WDR19 | Pig | short-rib thoracic dysplasia 9 with or without polydactyly | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saldino-Mainzer syndrome | ClinVar | PMID:25741868 more ... | WDR19 | Pig | Spermatogenic Failure 72 | | ISO | WDR19 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Spermatogenic failure 72 | ClinVar | PMID:17576681 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - MGI
Imported Disease Annotations - OMIM
Gene-Chemical Interaction Annotations Click to see Annotation Detail View
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
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