General description
enthält (15 Euro Patentgebühr für DM Exon2): Brachyurie (Stummelrute), Chondrodysplasie (CDPA) und -dystrophie (CDDY) (IVDD-Risiko), Degenerative Myelopathie (DM Exon2), Progressive Retinaatrophie (rcd3-PRA) und von Willebrand Erkrankung (vWD1)
Cardigan Welsh Corgi, Pembroke Welsh Corgi, Welsh Corgi (Cardigan/Pembroke)
Order details
Test number | 8661 |
Sample material | 0,5 ml EDTA Blut, 2x Backenabstrich, 1x Spezialabstrich (eNAT) |
Test duration | 7-14 Werktage |
Chondrodysplasie u. -dystrophie (CDDY & CDPA) (IVDD-Risiko)
Test specifications
Symptom complex | skeletal |
Causality | ursächlich |
Gene | FGF4 |
Mutation | COMPLEX |
Literature | OMIA:002542-9615 |
von Willebrand Erkrankung Typ I (vWD1)
Test specifications
Symptom complex | hämatologisch |
Causality | ursächlich |
Gene | VWF |
Mutation | G-A |
Literature | OMIA:001057-9615 |
Progressive Retinaatrophie (rcd3-PRA)
Test specifications
Symptom complex | ophtalmisch |
Age of onset | 6-16 Wochen |
Causality | ursächlich |
Gene | PDE6A |
Mutation | DEL |
Literature | OMIA:001314-9615 |
Degenerative Myelopathie (DM) Exon 2
Test specifications
Symptom complex | neuromuskulär |
Age of onset | ab 8 Jahre |
Causality | Hochrisikofaktor |
Gene | SOD1 |
Mutation | G-A |
Literature | OMIA:000263-9615 |
Brachyurie (Stummelrute)
Test specifications
Symptom complex | skeletal |
Age of onset | ab Geburt |
Causality | ursächlich |
Gene | TBXT |
Mutation | G-C |
Literature | OMIA:000975-9615 |