This tool looks for unlabeled Wikidata items in your language. It starts with a Wikidata item,
looks at all the associated Wikipedia pages, the links on all those pages, and lists the Wikidata items corresponding to the link targets.
Q2272470 - No label in !
Searching link targets on 11 Wikipedias...
Item | Label [] | Wikilabels | Link # |
---|---|---|---|
Q241953 [CC | ] | No label in ! | Mendelian Inheritance in Man | Online Mendelian Inheritance in Man | OMIM | الوراثة المندلية البشرية عبر الإنترنت | Herencia Mendeliana en el Hombre | 8 |
Q1360044 [CC | ] | No label in ! | Syndactylie | Syndactyly | Sindactilia | סינדקטיליה | Syndaktylia | Syndaktylie | Sindaktilija | 7 |
Q213103 [CC | ] | No label in ! | Diseases Database | قاعدة بيانات الأمراض | 6 |
Q371520 [CC | ] | No label in ! | Polydactylie | Polydactyly | Polidactilia | Polidaktylia | Polydaktylie | Polidaktilija | 6 |
Q1071953 [CC | ] | No label in ! | علم الوراثة الطبية | Medical genetics | Genética médica | גנטיקה רפואית | Genetica clinica | Medicinska genetika | 6 |
Q199897 [CC | ] | No label in ! | Medical Subject Headings | نظام فهرسة المواضيع الطبية | MeSH | 6 |
Q186380 [CC | ] | No label in ! | Autosom | Autosoom | Autosome | Autosomi | 5 |
Q378183 [CC | ] | No label in ! | Craniosynostose | Craneosinostosis | קרניוסינוסטוזיס | Kraniosynostose | Craniostenosi | 5 |
Q618246 [CC | ] | No label in ! | Syndroom van Apert | متلازمة أبير | Apert syndrome | Apert-Syndrom | Apertov sindrom | 5 |
Q45127 [CC | ] | No label in ! | ICD-10 | Międzynarodowa Klasyfikacja Chorób ICD-10 | 4 |
Q1286848 [CC | ] | No label in ! | Syndroom van Pfeiffer | متلازمة فايفر | Pfeiffer syndrome | Pfeifferov sindrom | 4 |
Q930752 [CC | ] | No label in ! | اختصاص طبي | Medical specialty | Especialidades médicas | Medicinska specijalnost | 4 |
Q12174 [CC | ] | No label in ! | سمنة | Obesity | Adipositas | Gojaznost | 4 |
Q42918 [CC | ] | No label in ! | Mutation | מוטציה | Mutacija | 4 |
Q1515833 [CC | ] | No label in ! | Orphanet | 4 |
Q183560 [CC | ] | No label in ! | إعاقة ذهنية | Intellectual disability | Kehitysvamma | 3 |
Q1786496 [CC | ] | No label in ! | تسنم الرأس وارتفاق الأصابع | Acrocephalosyndactyly | Kraniofaziale Fehlbildung | 3 |
Q510786 [CC | ] | No label in ! | صبغي 19 | Chromosom 19 (Mensch) | Hromosom 19 | 3 |
Q1770836 [CC | ] | No label in ! | متلازمة سوتو | Sotos syndrome | Sotosov sindrom | 3 |
Q2142496 [CC | ] | No label in ! | متلازمة سيلفر-روسل | Silver–Russell syndrome | Silver-Russellov sindrom | 3 |
Q208562 [CC | ] | No label in ! | متلازمة مارفان | Marfan syndrome | Marfanov sindrom | 3 |
Q540857 [CC | ] | No label in ! | Chromosome 6 | Chromosom 6 (Mensch) | Hromosom 6 | 3 |
Q3813599 [CC | ] | No label in ! | Turricephaly | Akrocefalia | Turmschädel | 3 |
Q13147 [CC | ] | No label in ! | Cráneo | Schädel | Lobanja | 3 |
Q7187 [CC | ] | No label in ! | Gen | גן (ביולוגיה) | 3 |
Q939364 [CC | ] | No label in ! | Synnynnäinen sydänvika | מום לב מולד | Herzfehler | 3 |
Q2737426 [CC | ] | No label in ! | Navelbreuk | Hernia umbilical | 2 |
Q18040527 [CC | ] | No label in ! | RAB23 | 2 |
Q323438 [CC | ] | No label in ! | أديم متوسط | Mesoderm | 2 |
Q1860 [CC | ] | No label in ! | اللغة الإنجليزية | אנגלית | 2 |
Q1323724 [CC | ] | No label in ! | انعدام الطرف | Ectromelia | 2 |
Q1153284 [CC | ] | No label in ! | تصقلب | Cyclopia | 2 |
Q1141026 [CC | ] | No label in ! | تكون المعيدة | Gastrulation | 2 |
Q727096 [CC | ] | No label in ! | عيب خلقي | Urođena mana | 2 |
Q179630 [CC | ] | No label in ! | متلازمة | Oireyhtymä | 2 |
Q303123 [CC | ] | No label in ! | متلازمة آرسكوغ-سكوت | Aarskog–Scott syndrome | 2 |
Q4681410 [CC | ] | No label in ! | متلازمة الإبهام المقرب | Adducted thumb syndrome | 2 |
Q1129947 [CC | ] | No label in ! | متلازمة التراجع الذيلي | Caudal regression syndrome | 2 |
Q209049 [CC | ] | No label in ! | متلازمة الحذف1q21.1 | 1q21.1 deletion syndrome | 2 |
Q2035109 [CC | ] | No label in ! | متلازمة الظفر والرضفة | Nail–patella syndrome | 2 |
Q521863 [CC | ] | No label in ! | متلازمة بكوث ودمان | Beckwith–Wiedemann syndrome | 2 |
Q1023604 [CC | ] | No label in ! | متلازمة تشارج | CHARGE syndrome | 2 |
Q202849 [CC | ] | No label in ! | متلازمة تيرنر | Turner syndrome | 2 |
Q3508705 [CC | ] | No label in ! | متلازمة تيموثي | Timothy syndrome | 2 |
Q769988 [CC | ] | No label in ! | متلازمة جولدينهار | Goldenhar syndrome | 2 |
Q574741 [CC | ] | No label in ! | متلازمة دوبويتز | Dubowitz syndrome | 2 |
Q2467739 [CC | ] | No label in ! | متلازمة دونوهيو | Donohue syndrome | 2 |
Q666980 [CC | ] | No label in ! | متلازمة روبينشتاين - تايبي | Rubinstein–Taybi syndrome | 2 |
Q1475743 [CC | ] | No label in ! | متلازمة روبينوف | Robinow syndrome | 2 |
Q8072143 [CC | ] | No label in ! | متلازمة زيمرمان–لاباند | Zimmermann–Laband syndrome | 2 |
Q3508686 [CC | ] | No label in ! | متلازمة ساثري - تشوتزين | Saethre–Chotzen syndrome | 2 |
Q998273 [CC | ] | No label in ! | متلازمة سميث-ليملي-أوبيتز | Smith–Lemli–Opitz syndrome | 2 |
Q1755537 [CC | ] | No label in ! | متلازمة فاكترل | VACTERL association | 2 |
Q1774750 [CC | ] | No label in ! | متلازمة كليبل-ترينوناي | Klippel–Trénaunay syndrome | 2 |
Q1133289 [CC | ] | No label in ! | متلازمة كورنيليا دي لانج | Cornelia de Lange syndrome | 2 |
Q914389 [CC | ] | No label in ! | متلازمة كوكاين | Cockayne syndrome | 2 |
Q1418152 [CC | ] | No label in ! | متلازمة موبيوس | Moebius syndrome | 2 |
Q1543446 [CC | ] | No label in ! | متلازمة نونان | Noonan syndrome | 2 |
Q182005 [CC | ] | No label in ! | متلازمة هولت-أورام | Holt–Oram syndrome | 2 |
Q4348144 [CC | ] | No label in ! | متلازمة ويفر | Weaver syndrome | 2 |
Q909442 [CC | ] | No label in ! | موسوعة كيوتو للجينات والمجينات | KEGG | 2 |
Q21127479 [CC | ] | No label in ! | Cole–Carpenter syndrome | Cole-Carpenter-Syndrom | 2 |
Q2888275 [CC | ] | No label in ! | Sakati–Nyhan–Tisdale syndrome | Síndrome de Sakati-Nyhan-Tisdale | 2 |
Q572169 [CC | ] | No label in ! | Seckel syndrome | Seckelov sindrom | 2 |
Q896643 [CC | ] | No label in ! | Braquidactilia | Brachydaktylie | 2 |
Q966052 [CC | ] | No label in ! | Criptorquidia | טמירות אשכים | 2 |
Q168291 [CC | ] | No label in ! | Córnea | Rožnjača | 2 |
Q938107 [CC | ] | No label in ! | Hipogonadismo | Hypogonadismus | 2 |
Q565 [CC | ] | No label in ! | Wikimedia Commons | ויקישיתוף | 2 |
Q50018 [CC | ] | No label in ! | ICD | Medicinske klasifikacije | 2 |
Q193003 [CC | ] | No label in ! | הידרוצפלוס | Idrocefalo | 2 |
Q200779 [CC | ] | No label in ! | פגם גנטי | Erbkrankheit | 2 |
Q39631 [CC | ] | No label in ! | Arts | 1 |
Q998 [CC | ] | No label in ! | Baby | 1 |
Q26513 [CC | ] | No label in ! | Foetus | 1 |
Q260263 [CC | ] | No label in ! | ICD10 Hoofdstuk XVII | 1 |
Q217690 [CC | ] | No label in ! | Incidentie | 1 |
Q229081 [CC | ] | No label in ! | Knieschijf | 1 |
Q324509 [CC | ] | No label in ! | Luxatie | 1 |
Q55 [CC | ] | No label in ! | Nederland | 1 |
Q779250 [CC | ] | No label in ! | Syndroom van Crouzon | 1 |
Q189082 [CC | ] | No label in ! | زرع الخلايا | 1 |
Q847102 [CC | ] | No label in ! | صبغي 12 | 1 |
Q840734 [CC | ] | No label in ! | صبغي 13 | 1 |
Q765245 [CC | ] | No label in ! | صبغي 15 | 1 |
Q638893 [CC | ] | No label in ! | صبغي 2 | 1 |
Q668633 [CC | ] | No label in ! | صبغي 3 | 1 |
Q836605 [CC | ] | No label in ! | صبغي 4 | 1 |
Q572848 [CC | ] | No label in ! | صبغي 8 | 1 |
Q131683 [CC | ] | No label in ! | علم الأجنة | 1 |
Q455338 [CC | ] | No label in ! | نظام اللغة الطبية الموحدة | 1 |
Q356188 [CC | ] | No label in ! | ADP ribosylation factor | 1 |
Q18053190 [CC | ] | No label in ! | ARL13B | 1 |
Q21097464 [CC | ] | No label in ! | ARL6 | 1 |
Q4712685 [CC | ] | No label in ! | Albright's hereditary osteodystrophy | 1 |
Q4812911 [CC | ] | No label in ! | Ataxia telangiectasia and Rad3 related | 1 |
Q3508616 [CC | ] | No label in ! | Baller–Gerold syndrome | 1 |
Q474254 [CC | ] | No label in ! | Bannayan–Riley–Ruvalcaba syndrome | 1 |
Q1678281 [CC | ] | No label in ! | Bardet–Biedl syndrome | 1 |
Q4887975 [CC | ] | No label in ! | Benign symmetric lipomatosis | 1 |
Q892776 [CC | ] | No label in ! | Bonnet–Dechaume–Blanc syndrome | 1 |
Q2280106 [CC | ] | No label in ! | Branchio-oto-renal syndrome | 1 |
Q423572 [CC | ] | No label in ! | Bruton's tyrosine kinase | 1 |
Q1022718 [CC | ] | No label in ! | CADASIL | 1 |
Q5008667 [CC | ] | No label in ! | CAMP-dependent pathway | 1 |
Q14912280 [CC | ] | No label in ! | CHEK2 | 1 |
Q1097490 [CC | ] | No label in ! | Cardiofaciocutaneous syndrome | 1 |
Q1044007 [CC | ] | No label in ! | Carney complex | 1 |
Q1052687 [CC | ] | No label in ! | Charcot–Marie–Tooth disease | 1 |
Q568865 [CC | ] | No label in ! | Cherubism | 1 |
Q959211 [CC | ] | No label in ! | Chylomicron retention disease | 1 |
Q1106881 [CC | ] | No label in ! | Coffin–Lowry syndrome | 1 |
Q2852249 [CC | ] | No label in ! | Congenital abnormality | 1 |
Q3242224 [CC | ] | No label in ! | Congenital generalized lipodystrophy | 1 |
Q5160441 [CC | ] | No label in ! | Congenital limb deformities | 1 |
Q1136492 [CC | ] | No label in ! | Costello syndrome | 1 |
Q1138188 [CC | ] | No label in ! | Cowden syndrome | 1 |
Q5182137 [CC | ] | No label in ! | Craniofacial abnormality | 1 |
Q5182142 [CC | ] | No label in ! | Craniofacial surgery | 1 |
Q3454555 [CC | ] | No label in ! | Dominance (genetics) | 1 |
Q18049853 [CC | ] | No label in ! | EDARADD | 1 |
Q5441566 [CC | ] | No label in ! | Feingold syndrome | 1 |
Q1425572 [CC | ] | No label in ! | Fraser syndrome | 1 |
Q3508635 [CC | ] | No label in ! | Fryns syndrome | 1 |
Q407438 [CC | ] | No label in ! | G protein | 1 |
Q14905160 [CC | ] | No label in ! | GNAS complex locus | 1 |
Q5514732 [CC | ] | No label in ! | GTP-binding protein regulators | 1 |
Q408592 [CC | ] | No label in ! | GTPase-activating protein | 1 |
Q18783658 [CC | ] | No label in ! | George Alfred Carpenter | 1 |
Q5609615 [CC | ] | No label in ! | Griscelli syndrome type 2 | 1 |
Q901088 [CC | ] | No label in ! | Guanine nucleotide exchange factor | 1 |
Q14884140 [CC | ] | No label in ! | HRAS | 1 |
Q408561 [CC | ] | No label in ! | Heterotrimeric G protein | 1 |
Q1077955 [CC | ] | No label in ! | Hypohidrotic ectodermal dysplasia | 1 |
Q14908209 [CC | ] | No label in ! | IKBKG | 1 |
Q884590 [CC | ] | No label in ! | Incontinentia pigmenti | 1 |
Q200303 [CC | ] | No label in ! | Inheritance | 1 |
Q1101694 [CC | ] | No label in ! | Joubert syndrome | 1 |
Q6318969 [CC | ] | No label in ! | Juvenile primary lateral sclerosis | 1 |
Q20969980 [CC | ] | No label in ! | KRAS | 1 |
Q6395632 [CC | ] | No label in ! | Keutel syndrome | 1 |
Q421851 [CC | ] | No label in ! | Kinase | 1 |
Q18036165 [CC | ] | No label in ! | LDB3 | 1 |
Q3961678 [CC | ] | No label in ! | Laurence–Moon syndrome | 1 |
Q1461101 [CC | ] | No label in ! | Lhermitte–Duclos disease | 1 |
Q187542 [CC | ] | No label in ! | Li–Fraumeni syndrome | 1 |
Q2628677 [CC | ] | No label in ! | Marinesco–Sjögren syndrome | 1 |
Q727008 [CC | ] | No label in ! | McCune–Albright syndrome | 1 |
Q410233 [CC | ] | No label in ! | Merlin (protein) | 1 |
Q6822414 [CC | ] | No label in ! | Metachondromatosis | 1 |
Q899651 [CC | ] | No label in ! | Mitogen-activated protein kinase | 1 |
Q1860507 [CC | ] | No label in ! | Myotonic dystrophy | 1 |
Q17914023 [CC | ] | No label in ! | Myotonin-protein kinase | 1 |
Q18029548 [CC | ] | No label in ! | Myotubularin 1 | 1 |
Q7616509 [CC | ] | No label in ! | Neurofibromatosis type I | 1 |
Q1935832 [CC | ] | No label in ! | Neurofibromatosis type II | 1 |
Q7003142 [CC | ] | No label in ! | Neutrophil immunodeficiency syndrome | 1 |
Q7049004 [CC | ] | No label in ! | Non-receptor tyrosine kinase | 1 |
Q7080278 [CC | ] | No label in ! | Oguchi disease | 1 |
Q7113674 [CC | ] | No label in ! | Overgrowth syndrome | 1 |
Q18040277 [CC | ] | No label in ! | PRKAG2 | 1 |
Q18030765 [CC | ] | No label in ! | PRKAR1A | 1 |
Q18030781 [CC | ] | No label in ! | PRKCSH | 1 |
Q416356 [CC | ] | No label in ! | PTEN (gene) | 1 |
Q14905494 [CC | ] | No label in ! | PTPN11 | 1 |
Q7169165 [CC | ] | No label in ! | Perlman syndrome | 1 |
Q1544989 [CC | ] | No label in ! | Peutz–Jeghers syndrome | 1 |
Q422476 [CC | ] | No label in ! | Phosphatase | 1 |
Q1756040 [CC | ] | No label in ! | Pierre Robin sequence | 1 |
Q246002 [CC | ] | No label in ! | Polycystic liver disease | 1 |
Q7248854 [CC | ] | No label in ! | Progressive osseous heteroplasia | 1 |
Q643602 [CC | ] | No label in ! | Protein tyrosine phosphatase | 1 |
Q281115 [CC | ] | No label in ! | Proteus syndrome | 1 |
Q7251694 [CC | ] | No label in ! | Proteus-like syndrome | 1 |
Q200745 [CC | ] | No label in ! | Pseudohypoaldosteronism | 1 |
Q819207 [CC | ] | No label in ! | Pseudohypoparathyroidism | 1 |
Q1477265 [CC | ] | No label in ! | Pseudopseudohypoparathyroidism | 1 |
Q7275015 [CC | ] | No label in ! | RAB27 | 1 |
Q18032651 [CC | ] | No label in ! | RAB7A | 1 |
Q18031005 [CC | ] | No label in ! | RAC2 | 1 |
Q18031288 [CC | ] | No label in ! | RPS6KA3 | 1 |
Q18031129 [CC | ] | No label in ! | Rhodopsin kinase | 1 |
Q18040027 [CC | ] | No label in ! | SAR1B | 1 |
Q41796999 [CC | ] | No label in ! | SH3BP2 | 1 |
Q1753883 [CC | ] | No label in ! | SNOMED CT | 1 |
Q2745322 [CC | ] | No label in ! | STK11 | 1 |
Q4857068 [CC | ] | No label in ! | Serine/threonine-specific protein kinase | 1 |
Q7502090 [CC | ] | No label in ! | Short stature | 1 |
Q5964993 [CC | ] | No label in ! | Signal transducing adaptor protein | 1 |
Q501128 [CC | ] | No label in ! | Single-nucleotide polymorphism | 1 |
Q795024 [CC | ] | No label in ! | Sirenomelia | 1 |
Q415071 [CC | ] | No label in ! | Small GTPase | 1 |
Q22965579 [CC | ] | No label in ! | Snyder–Robinson syndrome | 1 |
Q53160608 [CC | ] | No label in ! | Tatton-Brown–Rahman syndrome | 1 |
Q1362721 [CC | ] | No label in ! | Tuberous sclerosis | 1 |
Q18045861 [CC | ] | No label in ! | WNK1 | 1 |
Q18045874 [CC | ] | No label in ! | WNK4 | 1 |
Q1112752 [CC | ] | No label in ! | Watson syndrome | 1 |
Q925092 [CC | ] | No label in ! | Wolff–Parkinson–White syndrome | 1 |
Q283108 [CC | ] | No label in ! | X-linked agammaglobulinemia | 1 |
Q8041560 [CC | ] | No label in ! | X-linked intellectual disability | 1 |
Q3281380 [CC | ] | No label in ! | X-linked lymphoproliferative disease | 1 |
Q3331454 [CC | ] | No label in ! | X-linked myotubular myopathy | 1 |
Q20970121 [CC | ] | No label in ! | XIAP | 1 |
Q14907110 [CC | ] | No label in ! | ZAP70 | 1 |
Q8062938 [CC | ] | No label in ! | ZAP70 deficiency | 1 |
Q8067052 [CC | ] | No label in ! | Zaspopathy | 1 |
Q15729064 [CC | ] | No label in ! | Autosómico recesivo | 1 |
Q2856379 [CC | ] | No label in ! | Cifoescoliosis | 1 |
Q723530 [CC | ] | No label in ! | Clasificación Internacional de Atención Primaria | 1 |
Q838139 [CC | ] | No label in ! | Comunicación interventricular | 1 |
Q118455746 [CC | ] | No label in ! | Control de autoridades | 1 |
Q18419408 [CC | ] | No label in ! | Defecto septal ventricular | 1 |
Q579665 [CC | ] | No label in ! | Dextrocardia | 1 |
Q2072063 [CC | ] | No label in ! | Ductus arterioso persistente | 1 |
Q579527 [CC | ] | No label in ! | Estenosis pulmonar | 1 |
Q303231 [CC | ] | No label in ! | Genu valgo | 1 |
Q1886514 [CC | ] | No label in ! | Macrosomía | 1 |
Q223254 [CC | ] | No label in ! | Otitis media | 1 |
Q2834267 [CC | ] | No label in ! | Poliesplenia | 1 |
Q1416096 [CC | ] | No label in ! | Presión intracraneal | 1 |
Q1456383 [CC | ] | No label in ! | Situs inversus | 1 |
Q1126831 [CC | ] | No label in ! | Tetralogía de Fallot | 1 |
Q1758730 [CC | ] | No label in ! | Transposición de los grandes vasos | 1 |
Q2013 [CC | ] | No label in ! | Wikidata | 1 |
Q2057 [CC | ] | No label in ! | 1909 | 1 |
Q2019 [CC | ] | No label in ! | 2005 | 1 |
Q12133 [CC | ] | No label in ! | Kuurous | 1 |
Q11190 [CC | ] | No label in ! | Lääketiede | 1 |
Q170277 [CC | ] | No label in ! | Älykkyysosamäärä | 1 |
Q1057892 [CC | ] | No label in ! | גלילים | 1 |
Q182895 [CC | ] | No label in ! | הלסת העליונה | 1 |
Q37748 [CC | ] | No label in ! | כרומוזום | 1 |
Q1549382 [CC | ] | No label in ! | נשא (מחלה) | 1 |
Q1142806 [CC | ] | No label in ! | עיכוב התפתחותי | 1 |
Q112754 [CC | ] | No label in ! | Źródło pierwotne | 1 |
Q83360 [CC | ] | No label in ! | Daumen | 1 |
Q1182746 [CC | ] | No label in ! | Deformität | 1 |
Q641973 [CC | ] | No label in ! | Dentition | 1 |
Q25670 [CC | ] | No label in ! | Digital Object Identifier | 1 |
Q106227 [CC | ] | No label in ! | Genlocus | 1 |
Q1536720 [CC | ] | No label in ! | Gorlin-Goltz-Syndrom | 1 |
Q3508649 [CC | ] | No label in ! | Greig-Syndrom | 1 |
Q1641327 [CC | ] | No label in ! | Hypogenitalismus | 1 |
Q1568160 [CC | ] | No label in ! | Hypoplasie | 1 |
Q131276 [CC | ] | No label in ! | Internationale Standardnummer für fortlaufende Sammelwerke | 1 |
Q15832730 [CC | ] | No label in ! | Loss-of-Function-Mutation | 1 |
Q55011503 [CC | ] | No label in ! | Makrosomie | 1 |
Q769266 [CC | ] | No label in ! | Ontogenetische Entwicklung der Zähne | 1 |
Q123028 [CC | ] | No label in ! | Pädiatrie | 1 |
Q516266 [CC | ] | No label in ! | Rezessiv | 1 |
Q21030012 [CC | ] | No label in ! | Symmetrie (Geometrie) | 1 |
Q42106 [CC | ] | No label in ! | Synonym | 1 |
Q12136 [CC | ] | No label in ! | Malattia | 1 |
Q749409 [CC | ] | No label in ! | Osteogenesi imperfetta | 1 |
Q25554703 [CC | ] | No label in ! | Autosomno nasljeđivanje | 1 |
Q193211 [CC | ] | No label in ! | Cista | 1 |
Q9206884 [CC | ] | No label in ! | Dijagnostika | 1 |
Q16370 [CC | ] | No label in ! | Donja vilica | 1 |
Q285223 [CC | ] | No label in ! | Genetičko testiranje | 1 |
Q1641128 [CC | ] | No label in ! | Hipertelorizam | 1 |
Q40821 [CC | ] | No label in ! | Hirurgija | 1 |
Q1073 [CC | ] | No label in ! | Mozak | 1 |
Q179399 [CC | ] | No label in ! | Neplodnost | 1 |
Q7363 [CC | ] | No label in ! | Nos | 1 |
Q620207 [CC | ] | No label in ! | Prst | 1 |
Q24517852 [CC | ] | No label in ! | Ruka | 1 |
Q1072 [CC | ] | No label in ! | Srce | 1 |
Q15807 [CC | ] | No label in ! | Stopalo | 1 |
Q9384 [CC | ] | No label in ! | Testisi | 1 |
Q1345983 [CC | ] | No label in ! | Tvrdo nepce | 1 |
Q9633 [CC | ] | No label in ! | Vrat | 1 |
Q553 [CC | ] | No label in ! | Zub | 1 |
Q33767 [CC | ] | No label in ! | Šaka | 1 |