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- спіс артыкулаў у адным з праектаў Вікімедыя (be)
- ৱিকিপিডিয়া:ৰচনাশৈলীৰ হাতপুথি (as)
- บทความรายชื่อวิกิมีเดีย (th)
- විකිමීඩියා ලැයිස්තු ලිපිය (si)
- стаття-список у проєкті Вікімедіа (uk)
- Vikimedya liste maddesi (tr)
- Wikimedia leet airticle (sco)
- Wikimedia list article (en)
- Wikimedia liste (da)
- Wikimedia lysartikel (af)
- Wikimedia-Listn (ba)
- Wikimedia-Lëschtenartikel (lb)
- Wikimedia-lies (li)
- Wikimedia-lieste (zea)
- Wikimedia-lijst (nl)
- Wikimedia-list (fy)
- Wikimedia-listartikel (sv)
- Wikimedia-listeartikkel (nn)
- Wikimedia-luetteloartikkeli (fi)
- Wikimediako zerrenda artikulua (eu)
- article de llista de Wikimedia (ca)
- articlo de lista de Wikimedia (an)
- articol-listă în cadrul unui proiect Wikimedia (ro)
- artigo de listas da Wikimedia (gl)
- artikel daftar Wikimedia (in)
- artikull-listë e Wikimedias (sq)
- artículu de llista de Wikimedia (ast)
- bài viết danh sách Wikimedia (vi)
- lista d'un projècte Wikimèdia (oc)
- lista de un projecto de Wikimedia (ia)
- lista di Wikimedia (pap)
- lista di un progetto Wikimedia (it)
- lista w projekcie Wikimedia (pl)
- listartikolo en Vikimedio (eo)
- ojúewé àtojọ Wikimedia (yo)
- page de liste de Wikimédia (fr)
- popis na Wikimediji (hr)
- rencana senarai Wikimedia (ms)
- seznam Wikimedie (sl)
- seznam na projektech Wikimedia (cs)
- spisak na Wikimediji (bs)
- teunuléh dapeuta Wikimèdia (ace)
- zoznamový článok na projektu Wikimedia (sk)
- κατάλογος εγχειρήματος Wikimedia (el)
- উইকিমিডিয়ার তালিকা নিবন্ধ (bn)
- விக்கிப்பீடியா:பட்டியலிடல் (ta)
- Уикимедия списък (bg)
- саҳифаи феҳристӣ (tg)
- списак на Викимедији (sr)
- Վիքիմեդիայի նախագծի ցանկ (hy)
- список на статии на Викимедија (mk)
- וויקימעדיע ליסטע (ji)
- רשימת ערכים (iw)
- قائمة ويكيميديا (ar)
- статья-список в проекте Викимедиа (ru)
- ウィキメディアの一覧記事 (ja)
- 维基媒体列表条目 (zh)
- 위키미디어 목록 항목 (ko)
- Wikimedia-Liste (de)
- artículo de lista de Wikimedia (es)
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- dbr:Poland_syndrome
- dbr:Arteriovenous_fistula
- dbr:Arthrogryposis
- dbr:Von_Willebrand_disease
- dbr:Glycogen_storage_disease_type_V
- dbr:Multiple_endocrine_neoplasia
- dbr:Kernicterus
- dbr:Bardet–Biedl_syndrome
- dbr:Hydrops_fetalis
- dbr:Crigler–Najjar_syndrome
- dbr:Ehlers–Danlos_syndrome
- dbr:Familial_Mediterranean_fever
- dbr:POEMS_syndrome
- dbr:Scimitar_syndrome
- dbr:Platybasia
- dbr:Congenital_hypothyroidism
- dbr:Velopharyngeal_insufficiency
- dbr:Ebstein's_anomaly
- dbr:Amelogenesis_imperfecta
- dbr:Encephalocele
- dbr:Epispadias
- dbr:Hirschsprung's_disease
- dbr:Romano–Ward_syndrome
- dbr:Rothmund–Thomson_syndrome
- dbr:Tetralogy_of_Fallot
- dbr:Klippel–Feil_syndrome
- dbr:Glycogen_storage_disease_type_VI
- dbr:Prader–Willi_syndrome
- dbr:Lesch–Nyhan_syndrome
- dbr:CADASIL
- dbr:Charcot–Marie–Tooth_disease
- dbr:Pseudoxanthoma_elasticum
- dbr:Congenital_rubella_syndrome
- dbr:Meconium_aspiration_syndrome
- dbr:Sjögren–Larsson_syndrome
- dbr:Choroideremia
- dbr:Lactose_intolerance
- dbr:Retinopathy_of_prematurity
- dbr:Glycogen_storage_disease_type_I
- dbr:Hajdu–Cheney_syndrome
- dbr:Sickle_cell_trait
- dbr:Activated_protein_C_resistance
- dbr:Hermaphroditism
- dbr:Abetalipoproteinemia
- dbr:Meckel's_diverticulum
- dbr:Microcephaly
- dbr:United_States_National_Library_of_Medicine
- dbr:Xeroderma_pigmentosum
- dbc:Medical_Subject_Headings
- dbr:Hartnup_disease
- dbr:Medical_Subject_Headings
- dbr:Pseudohypoaldosteronism
- dbr:Turner_syndrome
- dbr:Glycogen_storage_disease_type_III
- dbr:Waardenburg_syndrome
- dbr:Syndactyly
- dbr:Tuberous_sclerosis
- dbr:Epidermolysis_bullosa
- dbr:Factor_XIII_deficiency
- dbr:Trilogy_of_Fallot
- dbr:Glycogen_storage_disease_type_II
- dbr:Hyperhomocysteinemia
- dbr:Kallmann_syndrome
- dbr:Synostosis
- dbr:Tricuspid_atresia
- dbr:Branchio-oto-renal_syndrome
- dbr:Pseudohermaphroditism
- dbr:Canavan_disease
- dbr:Jervell_and_Lange-Nielsen_syndrome
- dbr:Maple_syrup_urine_disease
- dbr:Alkaptonuria
- dbr:Glycogen_storage_disease
- dbr:Caroli_disease
- dbr:Cystinosis
- dbr:Multiple_endocrine_neoplasia_type_1
- dbr:Werner_syndrome
- dbr:Wolfram_syndrome
- dbr:Sphingolipidoses
- dbr:Factor_XII_deficiency
- dbr:Dwarfism
- dbr:Hydranencephaly
- dbr:Hydrocephalus
- dbr:Tourette_syndrome
- dbr:Progeria
- dbr:Gonadal_dysgenesis
- dbr:Severe_combined_immunodeficiency
- dbr:Port-wine_stain
- dbr:Gastroschisis
- dbr:Porphyria_cutanea_tarda
- dbr:Hypolipoproteinemia
- dbr:Oculocerebrorenal_syndrome
- dbr:Focal_dermal_hypoplasia
- dbr:Frasier_syndrome
- dbr:Aniridia
- dbr:Dentinogenesis_imperfecta
- dbr:Alexander_disease
- dbr:Cherubism
- dbr:Arachnoid_cyst
- dbr:Fabry_disease
- dbr:Hypokalemic_periodic_paralysis
- dbr:Rubinstein–Taybi_syndrome
- dbr:Ectodermal_dysplasia
- dbr:Ectromelia
- dbr:Wiskott–Aldrich_syndrome
- dbr:Bernard–Soulier_syndrome
- dbr:Pseudohypoparathyroidism
- dbr:Ectopia_lentis
- dbr:Antithrombin_III_deficiency
- dbr:Bronchogenic_cyst
- dbr:Alpha-mannosidosis
- dbr:Prune_belly_syndrome
- dbr:Tay–Sachs_disease
- dbr:Williams_syndrome
- dbr:Anencephaly
- dbr:Darier's_disease
- dbr:Dextrocardia
- dbr:Cystic_fibrosis
- dbr:Fucosidosis
- dbr:Refsum_disease
- dbr:DiGeorge_syndrome
- dbr:Ichthyosis
- dbr:Cryptorchidism
- dbr:Cystinuria
- dbr:Homocystinuria
- dbr:Smith–Lemli–Opitz_syndrome
- dbr:Pulmonary_atresia
- dbr:Septo-optic_dysplasia
- dbr:Machado–Joseph_disease
- dbr:Epidermolysis_bullosa_simplex
- dbr:Acatalasia
- dbr:Acrodermatitis
- dbr:Levocardia
- dbr:Thyroid_dysgenesis
- dbr:Bladder_exstrophy
- dbr:Albinism
- dbr:Double_outlet_right_ventricle
- dbr:Li–Fraumeni_syndrome
- dbr:Zellweger_syndrome
- dbr:Klinefelter_syndrome
- dbr:Marfan_syndrome
- dbr:Dyskeratosis_congenita
- dbr:Epidermolysis_bullosa_acquisita
- dbr:Laurence–Moon_syndrome
- dbr:Sclerema_neonatorum
- dbr:De_Lange_syndrome
- dbr:Pierre_Robin_syndrome
- dbr:Epidermolysis_bullosa,_junctional
- dbr:Epilepsy,_benign_neonatal
- dbr:Erythroblastosis,_fetal
- dbr:Adrenoleukodystrophy
- dbr:Angelman_syndrome
- dbr:Beckwith–Wiedemann_syndrome
- dbr:Cor_triatriatum
- dbr:Down_syndrome
- dbr:Esophageal_atresia
- dbr:Fragile_X_syndrome
- dbr:Gout
- dbr:Hypophosphatasia
- dbr:Lafora_disease
- dbr:Laron_syndrome
- dbr:Myotonic_dystrophy
- dbr:Noonan_syndrome
- dbr:Osteogenesis_imperfecta
- dbr:Polydactyly
- dbr:Wilms'_tumor
- dbr:Achondroplasia
- dbr:Biliary_atresia
- dbr:Choanal_atresia
- dbr:Friedreich's_ataxia
- dbr:Pseudopseudohypoparathyroidism
- dbr:Bloom_syndrome
- dbr:Coloboma
- dbr:Nesidioblastosis
- dbr:MERRF_syndrome
- dbr:Pelizaeus–Merzbacher_disease
- dbr:Mulibrey_nanism
- dbr:List_of_MeSH_codes
- dbr:List_of_MeSH_codes_(C15)
- dbr:List_of_MeSH_codes_(C17)
- dbr:Tracheobronchomegaly
- dbr:Sinus_pericranii
- dbr:Chorioamnionitis
- dbr:Cri_du_chat_syndrome
- dbr:Fanconi_anemia
- dbr:Fanconi_syndrome
- dbr:Neurofibromatosis
- dbr:Retinitis_pigmentosa
- dbr:Hereditary_fructose_intolerance
- dbr:Hypertelorism
- dbr:Hypoplastic_left_heart_syndrome
- dbr:Gardner's_syndrome
- dbr:Sturge–Weber_syndrome
- dbr:WAGR_syndrome
- dbr:Hypobetalipoproteinemia
- dbr:Aortopulmonary_septal_defect
- dbr:Proteus_syndrome
- dbr:Thalassemia
- dbr:Androgen_insensitivity_syndrome
- dbr:Blepharophimosis
- dbr:Incontinentia_pigmenti
- dbr:Bronchopulmonary_dysplasia
- dbr:Cockayne_syndrome
- dbr:Rett_syndrome
- dbr:Sandhoff_disease
- dbr:Anodontia
- dbr:Biotinidase_deficiency
- dbr:Denys–Drash_syndrome
- dbr:Goldenhar_syndrome
- dbr:Hermansky–Pudlak_syndrome
- dbr:Piebaldism
- dbr:Protein_C_deficiency
- dbr:Hypospadias
- dbr:Cutis_laxa
- dbr:Multicystic_dysplastic_kidney
- dbr:Multiple_carboxylase_deficiency
- dbr:Macrostomia
- dbr:Holoprosencephaly
- dbr:Situs_inversus
- dbr:Tangier_disease
- dbr:Citrullinemia
- dbr:Crisscross_heart
- dbr:Hemochromatosis
- dbr:Alpha-thalassemia
- dbr:Beta-mannosidosis
- dbc:Genetics-related_lists
- dbr:Prognathism
- dbr:Myotonia_congenita
- dbr:Alagille_syndrome
- dbr:Peutz–Jeghers_syndrome
- dbr:Glycogen_storage_disease_type_IV
- dbr:Coffin–Lowry_syndrome
- dbr:Micrognathism
- dbr:Retrognathism
- dbr:Nail–patella_syndrome
- dbr:Abnormalities
- dbr:Thanatophoric_dysplasia
- dbr:Central_nervous_system_cyst
- dbr:Holocarboxylase_synthetase_deficiency
- dbr:Lutembacher's_syndrome
- dbr:Porokeratosis
- dbr:Birth_trauma_(physical)
- dbr:Epidermolysis_bullosa_dystrophica
- dbr:Ichthyosis_vulgaris
- dbr:Intestinal_atresia
- dbr:Neural_tube_defects
- dbr:Meningocele
- dbr:Kartagener_syndrome
- dbr:MELAS_syndrome
- dbr:Dentin_dysplasia
- dbr:Freemartinism
- dbr:Monsters
- dbr:Aortic_coarctation
- dbr:Acidosis,_renal_tubular
- dbr:Dysplastic_nevus_syndrome
- dbr:Microstomia
- dbr:Retinal_dysplasia
- dbr:Acrocephalosyndactylia
- dbr:Lysosomal_storage_diseases
- dbr:Amniotic_band_syndrome
- dbr:Arnold–Chiari_malformation
- dbr:Möbius_syndrome
- dbr:Hydrophthalmos
- dbr:Arrhythmogenic_right_ventricular_dysplasia
- dbr:Huntington_disease
- dbr:Diaphragmatic_eventration
- dbr:Fuchs'_endothelial_dystrophy
- dbr:Neonatal_abstinence_syndrome
- dbr:Wolman_disease
- dbr:Adenomatous_polyposis_coli
- dbr:Factor_VII_deficiency
- dbr:Factor_X_deficiency
- dbr:Hyaline_membrane_disease
- dbr:Multiple_endocrine_neoplasia_type_2b
- dbr:Cleidocranial_dysplasia
- dbr:Leigh_disease
- dbr:Ellis–van_Creveld_syndrome
- dbr:Bronchopulmonary_sequestration
- dbr:Lingual_thyroid
- dbr:Lipid_metabolism,_inborn_errors
- dbr:Lipoidosis
- dbr:Lipoprotein_lipase_deficiency,_familial
- dbr:Thrombasthenia
- dbr:Cleft_palate
- dbr:Ductus_arteriosus,_patent
- dbr:Dysautonomia,_familial
- dbr:Dystonia_musculorum_deformans
- dbr:Eisenmenger_complex
- dbr:Ophthalmia_neonatorum
- dbr:Optic_atrophies,_hereditary
- dbr:Optic_atrophy,_autosomal_dominant
- dbr:Optic_atrophy,_hereditary,_leber
- dbr:Ornithine_carbamoyltransferase_deficiency_disease
- dbr:Orofaciodigital_syndromes
- dbr:Plagiocephaly,_nonsynostotic
- dbr:Fetal_alcohol_syndrome
- dbr:Hyperlipoproteinemia_type_III
- dbr:Dandy–Walker_syndrome
- dbr:Short_rib_–_polydactyly_syndrome
- dbr:Gilbert_disease
- dbr:Glucosephosphate_dehydrogenase_deficiency
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- no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually (en)
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| rdfs:label
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- List of MeSH codes (C16) (en)
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