http://dbpedia.org/resource/UDP_glucuronosyltransferase_1_family%2C_polypeptide_A1 +
, http://dbpedia.org/resource/Single-nucleotide_polymorphism +
, http://dbpedia.org/resource/Freeman%E2%80%93Sheldon_syndrome +
, http://dbpedia.org/resource/Larsen_syndrome +
, http://dbpedia.org/resource/Fragile_X_syndrome +
, http://dbpedia.org/resource/CDK13-related_disorder +
, http://dbpedia.org/resource/CAPOS_syndrome +
, http://dbpedia.org/resource/Androgen_insensitivity_syndrome +
, http://dbpedia.org/resource/Fast_parallel_proteolysis +
, http://dbpedia.org/resource/CCDC113 +
, http://dbpedia.org/resource/Okamoto_syndrome +
, http://dbpedia.org/resource/FOXL2 +
, http://dbpedia.org/resource/IDH2 +
, http://dbpedia.org/resource/Seymour_Benzer +
, http://dbpedia.org/resource/Adrenoleukodystrophy +
, http://dbpedia.org/resource/Bcr-Abl_tyrosine-kinase_inhibitor +
, http://dbpedia.org/resource/Folliculin +
, http://dbpedia.org/resource/Hypophosphatasia +
, http://dbpedia.org/resource/Treacher_Collins_syndrome +
, http://dbpedia.org/resource/Trimethylaminuria +
, http://dbpedia.org/resource/Li%E2%80%93Fraumeni_syndrome +
, http://dbpedia.org/resource/HSD17B10 +
, http://dbpedia.org/resource/Cyclic_nucleotide%E2%80%93gated_ion_channel +
, http://dbpedia.org/resource/Methylmalonyl-CoA_mutase +
, http://dbpedia.org/resource/Retinal_degeneration_%28rhodopsin_mutation%29 +
, http://dbpedia.org/resource/BARD1 +
, http://dbpedia.org/resource/Point_mutation +
, http://dbpedia.org/resource/Hypodysfibrinogenemia +
, http://dbpedia.org/resource/Hereditary_diffuse_leukoencephalopathy_with_spheroids +
, http://dbpedia.org/resource/Gilbert%27s_syndrome +
, http://dbpedia.org/resource/Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2_with_giant_axons +
, http://dbpedia.org/resource/Adenine_phosphoribosyltransferase +
, http://dbpedia.org/resource/Histidinemia +
, http://dbpedia.org/resource/BAP1 +
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