Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration PANK2 disease C1846582 CausalMutation 0.62 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration PANK2 disease C1846582 GeneticVariation 0.62 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration PANK2 disease C1846582 Biomarker 0.62 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration ANKS4B disease C1846582 Biomarker 0.01 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration PTN disease C1846582 Biomarker 0.01 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration SMARCAL1 disease C1846582 Biomarker 0.01 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration ANGPTL2 disease C1846582 Biomarker 0.01 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration AKR1B10 disease C1846582 Biomarker 0.01 disgenet
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration ANGPTL4 disease C1846582 Biomarker 0.01 disgenet
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