Matches in DBpedia 2014 for { ?s <http://dbpedia.org/ontology/omim> ?o. }
- Central_core_disease_of_muscle omim "117000".
- Centronuclear_myopathy omim "160150".
- Ceramide_synthase_4 omim "615334".
- Ceramide_synthase_5 omim "615335".
- Cerebral_arteriovenous_malformation omim "108010".
- Cerebral_dysgenesis%E2%80%93neuropathy%E2%80%93ichthyosis%E2%80%93keratoderma_syndrome omim "609528".
- Cerebral_palsy omim "603513".
- Cerebroretinal_microangiopathy_with_calcifications_and_cysts omim "612199".
- Cerebrotendineous_xanthomatosis omim "213700".
- Cervical_cancer omim "603956".
- Cervical_rib omim "117900".
- Ch%C3%A9diak%E2%80%93Higashi_syndrome omim "214500".
- Charcot%E2%80%93Marie%E2%80%93Tooth_disease omim "311860".
- Chemerin_peptide omim "601973".
- Cherubism omim "118400".
- Chicken_ovalbumin_upstream_promoter-transcription_factor omim "107773".
- Chicken_ovalbumin_upstream_promoter-transcription_factor omim "132890".
- Chimerin_1 omim "118423".
- Choanal_atresia omim "608911".
- Cholecystokinin_receptor omim "118444".
- Cholecystokinin_receptor omim "118445".
- Cholesteryl_ester_storage_disease omim "278000".
- Cholinesterase omim "100740".
- Cholinesterase omim "177400".
- Chondrocalcinosis omim "600668".
- Chondrosarcoma omim "215300".
- Chordin omim "603475".
- Chordoma omim "215400".
- Chorea_acanthocytosis omim "200150".
- Choroideremia omim "303100".
- Chromosome_5q_deletion_syndrome omim "153550".
- Chronic_granulomatous_disease omim "306400".
- Chronic_inflammatory_demyelinating_polyneuropathy omim "139393".
- Chronic_mucocutaneous_candidiasis omim "607644".
- Chronic_obstructive_pulmonary_disease omim "606963".
- Chronic_pancreatitis omim "167800".
- Chronic_progressive_external_ophthalmoplegia omim "157640".
- Chronic_recurrent_multifocal_osteomyelitis omim "259680".
- Chylomicron_retention_disease omim "246700".
- Chymase omim "118938".
- Cicatricial_pemphigoid omim "164185".
- Ciliary_neurotrophic_factor_receptor omim "118946".
- Citrate_synthase omim "118950".
- Citrin omim "603859".
- Citrullinemia omim "215700".
- Classification_of_transsexual_people omim "600952".
- Clathrin omim "118955".
- Clathrin omim "118970".
- Clathrin omim "601273".
- Cleidocranial_dysostosis omim "119600".
- Clouston's_hidrotic_ectodermal_dysplasia omim "129500".
- Club_foot omim "119800".
- Coarctation_of_the_aorta omim "120000".
- Coats'_disease omim "300216".
- Cocaine_and_amphetamine_regulated_transcript omim "602606".
- Cockayne_syndrome omim "216400".
- Coeliac_disease omim "212750".
- Coenzyme_Q10_deficiency omim "607426".
- Coffin%E2%80%93Lowry_syndrome omim "303600".
- Coffin%E2%80%93Siris_syndrome omim "135900".
- Cohen_syndrome omim "216550".
- Cold_urticaria omim "120100".
- Colitis omim "191390".
- Collagenase omim "120353".
- Collagenase omim "120355".
- Collectin_liver_1 omim "607620".
- Coloboma_of_optic_nerve omim "120430".
- Colorectal_cancer omim "114500".
- Common_variable_immunodeficiency omim "240500".
- Complement_2_deficiency omim "217000".
- Complement_3_deficiency omim "120700".
- Complement_4_deficiency omim "120820".
- Complement_component_1R omim "216950".
- Complement_component_1s omim "120580".
- Complement_component_4 omim "120810".
- Complement_component_4 omim "120820".
- Complement_component_5a omim "120900".
- Complement_component_7 omim "217070".
- Complement_component_9 omim "120940".
- Complement_deficiency omim "217000".
- Complement_receptor_of_the_immunoglobulin_family omim "300353".
- Complete_androgen_insensitivity_syndrome omim "312300".
- Cone_dystrophy omim "300085".
- Confluent_and_reticulated_papillomatosis omim "167900".
- Congenital_absence_of_the_vas_deferens omim "277180".
- Congenital_adrenal_hyperplasia omim "201910".
- Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency omim "202010".
- Congenital_adrenal_hyperplasia_due_to_17_alpha-hydroxylase_deficiency omim "202110".
- Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency omim "201910".
- Congenital_adrenal_hyperplasia_due_to_3_beta-hydroxysteroid_dehydrogenase_deficiency omim "201810".
- Congenital_afibrinogenemia omim "202400".
- Congenital_amegakaryocytic_thrombocytopenia omim "604498".
- Congenital_contractural_arachnodactyly omim "121050".
- Congenital_diaphragmatic_hernia omim "142340".
- Congenital_disorder_of_glycosylation omim "212065".
- Congenital_disorder_of_glycosylation_type_IIc omim "266265".
- Congenital_distal_spinal_muscular_atrophy omim "600175".
- Congenital_generalized_lipodystrophy omim "608594".
- Congenital_hypopituitarism omim "275200".
- Congenital_hypoplastic_anemia omim "609135".