Matches in DBpedia 2016-04 for { ?s <http://dbpedia.org/property/omim> ?o }
- 17-beta-hydroxysteroid_dehydrogenase_deficiency omim "264300".
- 17q21.31_microdeletion_syndrome omim "610443".
- 18p- omim "146390".
- 1p36_deletion_syndrome omim "607872".
- 1q21.1_deletion_syndrome omim "612474".
- 1q21.1_duplication_syndrome omim "612475".
- 2,4_Dienoyl-CoA_reductase omim "222745".
- 2,4_Dienoyl-CoA_reductase_deficiency omim "222745".
- 2-Hydroxyglutaric_aciduria omim "600721".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency omim "610006".
- 2-hydroxyphytanoyl-CoA_lyase omim "604300".
- 22q11.2_distal_deletion_syndrome omim "611867".
- 22q11.2_duplication_syndrome omim "608363".
- 22q13_deletion_syndrome omim "606232".
- 2q37_monosomy omim "600430".
- 3-Hydroxyacyl_ACP_dehydrase omim "607037".
- 3-M_syndrome omim "273750".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency omim "210200".
- 3-hydroxy-3-methylglutaryl-CoA_lyase omim "246450".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency omim "246450".
- 3-hydroxyacyl-CoA_dehydrogenase omim "601609".
- 3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency omim "601609".
- 3C_syndrome omim "220210".
- 3beta-Hydroxysteroid_dehydrogenase omim "109715".
- 3beta-Hydroxysteroid_dehydrogenase omim "613890".
- 3q29_microdeletion_syndrome omim "609425".
- 4-1BB_ligand omim "606182".
- 4-Hydroxyphenylpyruvate_dioxygenase omim "609695".
- 4-aminobutyrate_transaminase omim "137150".
- 5-3_exoribonuclease_1 omim "607994".
- 5-alpha-reductase_deficiency omim "264600".
- 5-alpha_reductase omim "184753".
- 5-alpha_reductase omim "607306".
- 6-phosphogluconate_dehydrogenase_deficiency omim "172200".
- 6-phosphogluconolactonase omim "604951".
- 9q34_deletion_syndrome omim "610253".
- ABCD_syndrome omim "600501".
- ACOT6 omim "614267".
- ALMS1 omim "606844".
- AL_amyloidosis omim "254500".
- APH-1 omim "607629".
- APH-1 omim "607630".
- APOA1BP omim "608862".
- AREDYLD_syndrome omim "207780".
- ATP-sensitive_potassium_channel omim "600509".
- ATP-sensitive_potassium_channel omim "600935".
- ATP-sensitive_potassium_channel omim "600937".
- ATP-sensitive_potassium_channel omim "601439".
- ATP2A2 omim "108740".
- ATP_citrate_lyase omim "108728".
- Aagenaes_syndrome omim "214900".
- Aarskog–Scott_syndrome omim "100050".
- Aase_syndrome omim "147800".
- Abdallat–Davis–Farrage_syndrome omim "270750".
- Abdominal_aortic_aneurysm omim "100070".
- Abetalipoproteinemia omim "200100".
- Ablepharon_macrostomia_syndrome omim "200110".
- Abruzzo–Erickson_syndrome omim "302905".
- Acanthosis_nigricans omim "100600".
- Acatalasia omim "115500".
- Accessory_auricle omim "610420".
- Accessory_breast omim "163700".
- Aceruloplasminemia omim "604290".
- Acetolactate_synthase omim "605770".
- Acetyl-CoA_C-acetyltransferase omim "100678".
- Acetyl-CoA_C-acetyltransferase omim "607809".
- Achalasia omim "200400".
- Achard_syndrome omim "100700".
- Acheiropodia omim "200500".
- Achondrogenesis omim "600972".
- Achondrogenesis_type_1B omim "600972".
- Achondrogenesis_type_2 omim "200610".
- Achondroplasia omim "100800".
- Achromatopsia omim "216900".
- Ackerman_syndrome omim "200970".
- Aconitase omim "100850".
- Aconitase omim "100880".
- Acrocallosal_syndrome omim "200990".
- Acrochordon omim "109400".
- Acrodermatitis_enteropathica omim "201100".
- Acrodysostosis omim "101800".
- Acrogeria omim "201200".
- Acrokeratoelastoidosis_of_Costa omim "101850".
- Acrokeratosis_verruciformis omim "101900".
- Acromegaly omim "102200".
- Acromicric_dysplasia omim "102370".
- Acropachy omim "119900".
- Acropectoral_syndrome omim "605967".
- Acro–dermato–ungual–lacrimal–tooth_syndrome omim "103285".
- Actinic_cheilitis omim "118330".
- Activated_protein_C_resistance omim "188055".
- Activating_protein_2 omim "107580".
- Activating_protein_2 omim "601601".
- Activating_protein_2 omim "601602".
- Activating_protein_2 omim "610161".
- Activin_and_inhibin omim "147290".
- Activin_and_inhibin omim "147380".
- Activin_and_inhibin omim "147390".
- Activin_and_inhibin omim "601233".
- Activin_and_inhibin omim "612031".