Matches in DBpedia 2014 for { ?s <http://dbpedia.org/ontology/omim> ?o. }
- Acyltransferase_like_2 omim "610472".
- Adams%E2%80%93Oliver_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".
- Adenine_phosphoribosyltransferase_deficiency omim "102600".
- Adenomyosis omim "600458".
- Adenosine_Monophosphate_Deaminase_Deficiency_type_1 omim "102770".
- Adenosine_deaminase_deficiency omim "102700".
- Adenosylhomocysteinase omim "180960".
- Adenylosuccinate_lyase_deficiency omim "103050".
- Adermatoglyphia omim "136000".
- Adiposis_dolorosa omim "103200".
- Adrenocortical_carcinoma omim "202300".
- Adrenocorticotropic_hormone omim "176830".
- Adrenocorticotropic_hormone_deficiency omim "201400".
- Adrenoleukodystrophy omim "300100".
- Adult-onset_basal_ganglia_disease omim "606159".
- African_iron_overload omim "601195".
- Agenesis_of_the_corpus_callosum omim "217990".
- Agouti_signalling_peptide omim "600201".
- Aicardi%E2%80%93Gouti%C3%A8res_syndrome omim "225750".
- Aicardi_syndrome omim "304050".
- Ainhum omim "103400".
- Alagille_syndrome omim "118450".
- Alanine_transaminase omim "138200".
- Albinism omim "203100".
- Albinism%E2%80%93deafness_syndrome omim "300700".
- Albright's_hereditary_osteodystrophy omim "103580".
- Aldolase_A_deficiency omim "611881".
- Alexander_disease omim "203450".
- Alkaptonuria omim "203500".
- Allan%E2%80%93Herndon%E2%80%93Dudley_syndrome omim "300523".
- Allergic_bronchopulmonary_aspergillosis omim "103920".
- Alopecia_areata omim "104000".
- Alpers'_disease omim "203700".
- Alpha-2-Macroglobulin omim "103950".
- Alpha-N-acetylglucosaminidase omim "609701".
- Alpha-mannosidosis omim "248500".
- Alpha-thalassemia omim "141800".
- Alpha-thalassemia_mental_retardation_syndrome omim "301040".
- Alpha_1-antitrypsin_deficiency omim "107400".
- Alpha_catenin omim "114025".
- Alpha_catenin omim "116805".
- Alpha_catenin omim "607667".
- Alport_syndrome omim "301050".
- Alstr%C3%B6m_syndrome omim "203800".
- Alternating_hemiplegia omim "602481".
- Alternating_hemiplegia_of_childhood omim "104290".
- Alveolar_capillary_dysplasia omim "265380".
- Alveolar_soft_part_sarcoma omim "606243".
- Alzheimer's_disease omim "104300".
- Amastia omim "113700".
- Amelogenin omim "300391".
- Amelogenin omim "410000".
- Amine_oxidase omim "104610".
- Amniotic_band_constriction omim "217100".
- Amyotrophic_lateral_sclerosis omim "105400".
- Andersen%E2%80%93Tawil_syndrome omim "170390".
- Androgen-binding_protein omim "182205".
- Androgen_insensitivity_syndrome omim "312300".
- Anencephaly omim "206500".
- Aneurysmal_bone_cyst omim "606179".
- Angelman_syndrome omim "105830".
- Angioedema omim "606860".
- Angiopoietin omim "601667".
- Angiopoietin omim "601922".
- Angiopoietin_receptor omim "600221".
- Angiopoietin_receptor omim "600222".
- Angiotensin_receptor omim "106165".
- Angiotensin_receptor omim "300034".
- Aniridia omim "106200".
- Anisocoria omim "106240".
- Ankylosing_spondylitis omim "106300".
- Ankyrin omim "106410".
- Ankyrin omim "182900".
- Ankyrin omim "600465".
- Annular_pancreas omim "167750".
- Anorchia omim "273250".
- Anorexia_nervosa omim "606788".
- Anorexia_nervosa_(differential_diagnoses) omim "606788".
- Anterior_ischemic_optic_neuropathy omim "258660".
- Anterior_segment_mesenchymal_dysgenesis omim "107250".
- Anti-M%C3%BCllerian_hormone omim "600956".
- Anti-M%C3%BCllerian_hormone omim "600957".
- Anti-M%C3%BCllerian_hormone_receptor omim "600956".
- Antiphospholipid_syndrome omim "107320".
- Antithrombin_III_deficiency omim "613118".
- Antley%E2%80%93Bixler_syndrome omim "207410".
- Aortic_aneurysm omim "100070".
- Aortic_dissection omim "607086".
- Apert_syndrome omim "101200".
- Aphakia omim "610256".
- Aplasia_cutis_congenita omim "107600".
- Aplastic_anemia omim "609135".
- Apolipoprotein_A2 omim "107670".
- Apolipoprotein_B_deficiency omim "107730".
- Apoptosis-inducing_factor omim "300169".