"phenotype1" (e.g., "Mandibular prognathia")
"disease1" (e.g., Kabuki syndrome 1)
"inheritance mode1" (e.g., Autosomal dominant);
"coordinate1" (e.g., chr11:2686616)
"variant" (e.g., chr1:27089776G>T)
"range1" (e.g., chr11:2686616-2886620)
"cnv_size:size1" (e.g., cnv_size:100000-10000000)
"gene1" (e.g., BRCA1)
"gene1, gene2, gene3" (e.g., BRCA1, BRCA2, UBE3A)