Matches in DBpedia 2015-10 for { ?s <http://dbpedia.org/ontology/omim> ?o }
- 17-beta-hydroxysteroid_dehydrogenase_deficiency omim "264300".
- 17q21.31_microdeletion_syndrome omim "610443".
- 18p- omim "146390".
- 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".
- 3C_syndrome omim "220210".
- 3q29_microdeletion_syndrome omim "609425".
- 4-1BB_ligand omim "606182".
- 5-alpha-reductase_deficiency omim "264600".
- 6-phosphogluconate_dehydrogenase_deficiency omim "172200".
- 6-phosphogluconolactonase omim "604951".
- 9q34_deletion_syndrome omim "610253".
- ABCD_syndrome omim "600501".
- ACADVL omim "609575".
- ACOT6 omim "614267".
- ALDH8A1 omim "606467".
- 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".
- Abdallat–Davis–Farrage_syndrome omim "270750".
- Abdominal_aortic_aneurysm omim "100070".
- Abetalipoproteinemia omim "200100".
- Abruzzo–Erickson_syndrome omim "302905".
- Acanthosis_nigricans omim "100600".
- Acatalasia omim "115500".
- Accessory_auricle omim "610420".
- Accessory_breast omim "163700".
- Aceruloplasminemia omim "604290".
- Achalasia omim "200400".
- Acheiropodia omim "200500".
- Achondrogenesis omim "600972".
- Achondrogenesis_type_1B omim "600972".
- Achondroplasia omim "100800".
- Achromatopsia omim "216900".
- Ackerman_syndrome omim "200970".
- 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".
- 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".
- Activin_type_2_receptors omim "102581".
- Activin_type_2_receptors omim "602730".
- Acute_erythroid_leukemia omim "133180".
- Acute_fatty_liver_of_pregnancy omim "609016".
- Acute_intermittent_porphyria omim "176000".
- Acute_interstitial_pneumonitis omim "178500".
- Acute_myeloid_leukemia omim "602439".
- Acute_promyelocytic_leukemia omim "102578".
- Acyl-CoA:lysocardiolipin_acyltransferase-1 omim "614241".
- Acyltransferase_like_2 omim "610472".
- Adams–Oliver_syndrome omim "100300".
- Adducted_thumb_syndrome omim "201550".
- Adducted_thumbs_syndrome omim "201550".
- Adenine_nucleotide_translocator omim "103220".
- Adenine_nucleotide_translocator omim "300150".
- Adenine_nucleotide_translocator omim "403000".
- Adenomyosis omim "600458".
- Adenosine_deaminase_deficiency omim "102700".
- Adenosine_monophosphate_deaminase_deficiency_type_1 omim "102770".
- Adenosylhomocysteinase omim "180960".
- Adenylosuccinate_lyase_deficiency omim "103050".