Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Robinow syndrome, autosomal recessive ROR2 disease C1849334 CausalMutation 1 orphanet , disgenet
Robinow syndrome, autosomal recessive ROR2 disease C1849334 GeneticVariation 1 orphanet , disgenet
Robinow syndrome, autosomal recessive ROR2 disease C1849334 Biomarker 1 orphanet , disgenet
Robinow syndrome, autosomal recessive NXN disease C1849334 GermlineCausalMutation 0.3 orphanet , disgenet
Robinow syndrome, autosomal recessive PRICKLE1 disease C1849334 Biomarker 0.2 disgenet
Robinow syndrome, autosomal recessive PTCH1 disease C1849334 GeneticVariation 0.01 disgenet
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