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.
Q1707822 - Pendred syndrome
Searching link targets on 13 Wikipedias...
| Item | Label [en] | Wikilabels | Link # |
|---|---|---|---|
Q12133 [CC |  ] | deafness | Gehörlosigkeit | Głuchota | Surdité | Deafness | Sordera | Kuurous | صمم | Глувост | Gluhoća | 9 |
| Q165135 [CC | ] | goiter | Goitre | Struma | Wole (tarczyca) | Зоб (заболевание) | Bocio | Schildkliervergroting | Struma (endocrinologia) | Gušavost | 9 |
| Q241953 [CC | ] | Online Mendelian Inheritance in Man | Mendelian Inheritance in Man | Менделевское наследование у человека | Héritage mendélien chez l'humain | Online Mendelian Inheritance in Man | Herencia Mendeliana en el Hombre | الوراثة المندلية البشرية عبر الإنترنت | OMIM | 9 |
| Q42918 [CC | ] | mutation | Mutacja | Mutation | Mutación | Mutaatio | Mutazione genetica | طفرة (أحياء) | Мутација | Mutacija | 8 |
| Q200779 [CC | ] | genetic disease | Erbkrankheit | Maladie génétique | Genetic disorder | Erfelijke aandoening | Malattia genetica | اضطراب جيني | Genetički poremećaj | 7 |
| Q16501 [CC | ] | hypothyroidism | Hypothyreose | Гипотиреоз | Hypothyroïdie | Hipotiroidismo | Hypothyreoïdie | Ipotiroidismo | قصور الدرقية | 7 |
| Q657319 [CC | ] | human chromosome 7 | Chromosom 7 (Mensch) | Chromosom 7 | Chromosome 7 humain | Cromosoma 7 | صبغي 7 | Hromosom 7 | 6 |
| Q317857 [CC | ] | cochlea | Hörschnecke | Cochlea | Cóclea | Coclea (anatomia) | قوقعة (تشريح) | Pužnica | 6 |
| Q213103 [CC | ] | Diseases Database | Diseases Database | قاعدة بيانات الأمراض | 6 |
| Q16399 [CC | ] | thyroid gland | Щитовидная железа | Thyroid | Kilpirauhanen | Tiroide | غدة درقية | Штитна жлезда | 6 |
| Q45127 [CC | ] | International Classification of Diseases, Tenth Revision (ICD-10) | ICD-10 | МКБ-10 | MKB 10 | 5 |
| Q199897 [CC | ] | Medical Subject Headings | Medical Subject Headings | نظام فهرسة المواضيع الطبية | 5 |
| Q162606 [CC | ] | endocrinology | Эндокринология | Endocrinology | Endocrinología | Endocrinologia | علم الغدد الصم | 5 |
| Q7187 [CC | ] | gene | Gene | Gène | Ген | Gen | 5 |
| Q25670 [CC | ] | digital object identifier | Digital Object Identifier | DOI (identyfikator cyfrowy) | Digital object identifier | معرف الغرض الرقمي | 4 |
| Q1103 [CC | ] | iodine | Jod | Iod | يود | 4 |
| Q939416 [CC | ] | The Lancet | The Lancet | 4 |
| Q422106 [CC | ] | thyroid hormone | Hormony tarczycy | Тиреоидные гормоны | Hormona tiroidea | Tireoidni hormoni | 4 |
| Q212344 [CC | ] | inner ear | Ucho wewnętrzne | Oído interno | أذن داخلية | Unutrašnje uho | 4 |
| Q179815 [CC | ] | Durham | Durham | Durham, England | درم (إنجلترا) | 4 |
| Q9377 [CC | ] | kidney | Kidney | Riñón | كلية | Бубрег | 4 |
| Q161238 [CC | ] | magnetic resonance imaging | Magnetic resonance imaging | Imaging a risonanza magnetica | تصوير بالرنين المغناطيسي | Магнетна резонанција | 4 |
| Q24786398 [CC | ] | Pendrin | Pendrin | 3 |
| Q178694 [CC | ] | heredity | Vererbung (Biologie) | Ereditarietà genetica | Nasljeđivanje | 3 |
| Q455 [CC | ] | Encyclopædia Britannica | Encyklopedia Britannica | Enciclopedia Británica | Enciclopedia Britannica | 3 |
| Q2082879 [CC | ] | PubMed ID | PMID | 3 |
| Q727096 [CC | ] | congenital disorder | Wady wrodzone | Malattia congenita | عيب خلقي | 3 |
| Q531012 [CC | ] | congenital hypothyroidism | Wrodzona niedoczynność tarczycy | Congenital hypothyroidism | قصور الغدة الدرقية الخلقي | 3 |
| Q15729064 [CC | ] | autosomal recessive | Аутосомно-рецессивный тип наследования | Transmission autosomique récessive | Autosómico recesivo | 3 |
| Q1586088 [CC | ] | hypoparathyroidism | Гипопаратиреоз | Hypoparathyroidism | قصور جارات الدرقية | 3 |
| Q156871 [CC | ] | pituitary gland | Гипофиз | Pituitary gland | غدة نخامية | 3 |
| Q11364 [CC | ] | hormone | Гормоны | هرمون | Hormon | 3 |
| Q712294 [CC | ] | adrenal gland | Надпочечники | Adrenal gland | غدة كظرية | 3 |
| Q650401 [CC | ] | parathyroid | Паращитовидные железы | Parathyroid gland | غدة جارة الدرقية | 3 |
| Q216852 [CC | ] | thyroxine | Тироксин | Tiroxina | ثيروكسين | 3 |
| Q37748 [CC | ] | chromosome | Хромосома | Chromosome | Kromosomi | 3 |
| Q1515833 [CC | ] | Orphanet | Orphanet | 3 |
| Q409202 [CC | ] | bicarbonate ion | Bicarbonate | بيكربونات | Bikarbonat | 3 |
| Q22890 [CC | ] | Ireland | Ireland | جزيرة أيرلندا | Ирска (остров) | 3 |
| Q930752 [CC | ] | medical specialty | Medical specialty | Especialidades médicas | اختصاص طبي | 3 |
| Q16035842 [CC | ] | hearing loss | Slechthorendheid | فقدان السمع | Gubitak sluha | 3 |
| Q1568160 [CC | ] | hypoplasia | Hypoplasie | 2 |
| Q516266 [CC | ] | recessive trait | Rezessiv | صفة متنحية | 2 |
| Q169872 [CC | ] | symptom | Symptom | Sintomo | 2 |
| Q179630 [CC | ] | syndrome | Syndrom | متلازمة | 2 |
| Q1944248 [CC | ] | Mondini dysplasia | Dysplazja Mondiniego | Mondini dysplasia | 2 |
| Q11094 [CC | ] | chronic thyroiditis | Аутоиммунный тиреоидит | Ziekte van Hashimoto | 2 |
| Q55695727 [CC | ] | ICD-11 | МКБ-11 | CIE-11 | 2 |
| Q50018 [CC | ] | International Statistical Classification of Diseases and Related Health Problems | Международная классификация болезней | Medicinske klasifikacije | 2 |
| Q928697 [CC | ] | sensorineural hearing loss | Нейросенсорная тугоухость | Sensorineural hearing loss | 2 |
| Q922411 [CC | ] | hypopituitarism | Пангипопитуитаризм | قصور النخامية | 2 |
| Q826522 [CC | ] | thyroid cancer | Рак щитовидной железы | Kilpirauhassyöpä | 2 |
| Q4669713 [CC | ] | absent adrenal gland | Absent adrenal gland | غياب الغدة الكظرية | 2 |
| Q842438 [CC | ] | British | British people | Британци | 2 |
| Q2661443 [CC | ] | endocrine system disease | Endocrine disease | أمراض الغدد الصماء | 2 |
| Q3048291 [CC | ] | GeneReviews | GeneReviews | 2 |
| Q285223 [CC | ] | genetic testing | Genetic testing | Genetičko testiranje | 2 |
| Q7170423 [CC | ] | Persistent thyroglossal duct | Persistent thyroglossal duct | قناة درقية لسانية مستديمة | 2 |
| Q6842789 [CC | ] | sensitivity | Sensitivity (test) | Sensibilità (statistica) | 2 |
| Q502785 [CC | ] | thyroglossal cyst | Thyroglossal cyst | كيس درقي لساني | 2 |
| Q6673122 [CC | ] | thyroid gland disease | Thyroid disease | مرض الدرقية | 2 |
| Q7799746 [CC | ] | thyroid dysgenesis | Thyroid dysgenesis | خلل تكون الغدة الدرقية | 2 |
| Q7799748 [CC | ] | Thyroid dyshormonogenesis | Thyroid dyshormonogenesis | خلل تكون هرمونات الدرقية | 2 |
| Q186380 [CC | ] | autosome | Autosomi | صبغي جسمي | 2 |
| Q39631 [CC | ] | physician | Arts | Medico | 2 |
| Q27 [CC | ] | Republic of Ireland | Irlanda | Irska | 2 |
| Q188952 [CC | ] | medical history | Anamnese | 1 |
| Q837512 [CC | ] | differential diagnosis | Differenzialdiagnose | 1 |
| Q8047 [CC | ] | enzyme | Enzym | 1 |
| Q1378628 [CC | ] | No label in en! | Euthyreose | 1 |
| Q843863 [CC | ] | genetic linkage | Genkopplung | 1 |
| Q131276 [CC | ] | International Standard Serial Number | Internationale Standardnummer für fortlaufende Sammelwerke | 1 |
| Q15724418 [CC | ] | No label in en! | Medizinische Genetik (Zeitschrift) | 1 |
| Q2070176 [CC | ] | No label in en! | Perchlorat-Depletions-Test | 1 |
| Q419502 [CC | ] | Thyroid peroxidase | Thyreoperoxidase | 1 |
| Q2111029 [CC | ] | transport protein | Transportprotein | 1 |
| Q2421877 [CC | ] | labyrinth | Błędnik (anatomia) | 1 |
| Q10267817 [CC | ] | autosomal recessive disease | Dziedziczenie autosomalne recesywne | 1 |
| Q615699 [CC | ] | online encyclopedia | Encyklopedia internetowa | 1 |
| Q1860 [CC | ] | English | Język angielski | 1 |
| Q1057 [CC | ] | metabolism | Metabolizm | 1 |
| Q11819940 [CC | ] | No label in en! | Pobudliwość | 1 |
| Q1153641 [CC | ] | Wolfram syndrome | DIDMOAD-синдром | 1 |
| Q746413 [CC | ] | Elsevier BV | Elsevier | 1 |
| Q976454 [CC | ] | Nature Genetics | Nature Genetics | 1 |
| Q4057495 [CC | ] | parathyroid adenoma | Аденома паращитовидной железы | 1 |
| Q132621 [CC | ] | epinephrine | Адреналин | 1 |
| Q189580 [CC | ] | acromegaly | Акромегалия | 1 |
| Q184564 [CC | ] | aldosterone | Альдостерон | 1 |
| Q65963433 [CC | ] | angiotensins | Ангиотензин | 1 |
| Q2817108 [CC | ] | androstenediol | Андростендиол | 1 |
| Q422469 [CC | ] | androsterone | Андростерон | 1 |
| Q21124841 [CC | ] | arginine vasopressin | Антидиуретический гормон | 1 |
| Q3621073 [CC | ] | Apudoma | Апудома | 1 |
| Q675311 [CC | ] | autoimmune polyendocrine syndrome | Аутоиммунный полиэндокринный синдром | 1 |
| Q8282 [CC | ] | Addison's disease | Болезнь Аддисона | 1 |
| Q4090776 [CC | ] | Simmonds' cachexia | Болезнь Симмондса | 1 |
| Q414964 [CC | ] | vasoactive intestinal peptide | Вазоактивный интестинальный пептид | 1 |
| Q366868 [CC | ] | congenital adrenal hyperplasia | Врождённая гиперплазия коры надпочечников | 1 |
| Q407181 [CC | ] | Gastrin | Гастрин | 1 |
| Q4134132 [CC | ] | No label in en! | Гастроэнтеропанкреатическая эндокринная система | 1 |
| Q1640860 [CC | ] | hyperaldosteronism | Гиперальдостеронизм | 1 |
| Q4138723 [CC | ] | acute hypercalcemia | Гиперкальциемический криз | 1 |
| Q1344835 [CC | ] | hyperparathyroidism | Гиперпаратиреоз | 1 |
| Q1433936 [CC | ] | hyperprolactinemia | Гиперпролактинемия | 1 |
| Q16499 [CC | ] | hyperthyroidism | Гипертиреоз | 1 |
| Q4138771 [CC | ] | list of causes of hypoglycemia | Гипогликемический синдром | 1 |
| Q938107 [CC | ] | hypogonadism | Гипогонадизм | 1 |
| Q4138773 [CC | ] | hypocalcemic crisis | Гипокальциемический криз | 1 |
| Q2507454 [CC | ] | adrenal insufficiency | Гипокортицизм | 1 |
| Q164386 [CC | ] | hypothalamus | Гипоталамус | 1 |
| Q1118643 [CC | ] | deaf-mute | Глухонемота | 1 |
| Q170617 [CC | ] | glucagon | Глюкагон | 1 |
| Q770843 [CC | ] | glucagonoma | Глюкагонома | 1 |
| Q22677256 [CC | ] | gastric inhibitory polypeptide | Глюкозозависимый инсулинотропный полипептид | 1 |
| Q213456 [CC | ] | gonad | Гонады | 1 |
| Q29956617 [CC | ] | growth hormone | Гормон роста | 1 |
| Q422269 [CC | ] | ghrelin | Грелин | 1 |
| Q408376 [CC | ] | dehydroepiandrosterone | Дегидроэпиандростерон | 1 |
| Q411054 [CC | ] | dihydrotestosterone | Дигидротестостерон | 1 |
| Q371168 [CC | ] | diffuse neuroendocrine system | Диффузная нейроэндокринная система | 1 |
| Q749637 [CC | ] | corpus luteum | Жёлтое тело | 1 |
| Q50265665 [CC | ] | insulin | Инсулин | 1 |
| Q1501239 [CC | ] | insulinoma | Инсулинома | 1 |
| Q933444 [CC | ] | islet-cell adenoma | Инсулома | 1 |
| Q190875 [CC | ] | cortisol | Кортизол | 1 |
| Q423185 [CC | ] | cortisone | Кортизон | 1 |
| Q210420 [CC | ] | corticosteroid | Кортикостероиды | 1 |
| Q422543 [CC | ] | corticosterone | Кортикостерон | 1 |
| Q424190 [CC | ] | leukotriene | Лейкотриены | 1 |
| Q223739 [CC | ] | leptin | Лептин | 1 |
| Q50265477 [CC | ] | glyco-Lutropin [extracellular region] | Лютеинизирующий гормон | 1 |
| Q423981 [CC | ] | melanocyte-stimulating hormone | Меланоцитстимулирующие гормоны | 1 |
| Q180912 [CC | ] | melatonin | Мелатонин | 1 |
| Q657193 [CC | ] | metabolic syndrome | Метаболический синдром | 1 |
| Q4291495 [CC | ] | antipsychotic-induced metabolic syndrome | Метаболический синдром и антипсихотики | 1 |
| Q421768 [CC | ] | methyltestosterone | Метилтестостерон | 1 |
| Q966229 [CC | ] | myxedema | Микседема | 1 |
| Q1553018 [CC | ] | multiple endocrine neoplasia | Множественная эндокринная неоплазия | 1 |
| Q1535394 [CC | ] | nesidioblastosis | Незидиобластоз | 1 |
| Q162657 [CC | ] | neurotransmitter | Нейромедиатор | 1 |
| Q7616509 [CC | ] | neurofibromatosis type I | Нейрофиброматоз I типа | 1 |
| Q131749 [CC | ] | anorexia nervosa | Нервная анорексия | 1 |
| Q220551 [CC | ] | diabetes insipidus | Несахарный диабет | 1 |
| Q845300 [CC | ] | nosology | Нозология | 1 |
| Q186242 [CC | ] | norepinephrine | Норадреналин | 1 |
| Q728309 [CC | ] | islet of Langerhans | Островки Лангерганса | 1 |
| Q424233 [CC | ] | suppurative thyroiditis | Острый тиреоидит | 1 |
| Q4341094 [CC | ] | PPoma | ППома | 1 |
| Q246978 [CC | ] | pancreatic polypeptide | Панкреатический полипептид | 1 |
| Q416997 [CC | ] | peptide hormone | Пептидные гормоны | 1 |
| Q1047551 [CC | ] | pinealoma | Пинеалома | 1 |
| Q1960869 [CC | ] | placental lactogen | Плацентарный лактоген | 1 |
| Q4368173 [CC | ] | subacute thyroiditis | Подострый тиреоидит | 1 |
| Q422812 [CC | ] | sex steroid | Половые гормоны | 1 |
| Q16488 [CC | ] | postpartum thyroiditis | Послеродовой тиреоидит | 1 |
| Q2700511 [CC | ] | pregnane | Прегнан | 1 |
| Q2087205 [CC | ] | prediabetes syndrome | Предиабет | 1 |
| Q11426176 [CC | ] | prednisolone | Преднизолон | 1 |
| Q78185357 [CC | ] | atrial natriuretic peptide | Предсердный натрийуретический пептид | 1 |
| Q26963 [CC | ] | progesterone | Прогестерон | 1 |
| Q66590068 [CC | ] | prolactin | Пролактин | 1 |
| Q209717 [CC | ] | prostaglandins | Простагландины | 1 |
| Q412050 [CC | ] | prostacyclin | Простациклин | 1 |
| Q1339466 [CC | ] | empty sella syndrome | Пустое турецкое седло | 1 |
| Q24773888 [CC | ] | Relaxin | Релаксин | 1 |
| Q12206 [CC | ] | diabetes | Сахарный диабет | 1 |
| Q422301 [CC | ] | secretin | Секретин | 1 |
| Q167934 [CC | ] | serotonin | Серотонин | 1 |
| Q4347774 [CC | ] | autoimmune polyendocrine syndrome type 1 | Синдром MEDAC | 1 |
| Q2666433 [CC | ] | MELAS syndrome | Синдром MELAS | 1 |
| Q432814 [CC | ] | Alström syndrome | Синдром Альстрёма | 1 |
| Q790971 [CC | ] | Bartter disease | Синдром Барттера | 1 |
| Q3347154 [CC | ] | multiple endocrine neoplasia type 1 | Синдром Вермера | 1 |
| Q218712 [CC | ] | Zollinger–Ellison syndrome | Синдром Золлингера — Эллисона | 1 |
| Q1165179 [CC | ] | Kallmann syndrome | Синдром Каллмана | 1 |
| Q1044007 [CC | ] | Carney complex | Синдром Карнея | 1 |
| Q4420123 [CC | ] | Kylin syndrome | Синдром Килина | 1 |
| Q207133 [CC | ] | Klinefelter's syndrome | Синдром Клайнфельтера | 1 |
| Q1482922 [CC | ] | Conn's syndrome | Синдром Конна | 1 |
| Q669822 [CC | ] | Laron syndrome | Синдром Ларона | 1 |
| Q1823656 [CC | ] | Liddle syndrome | Синдром Лиддла | 1 |
| Q4420126 [CC | ] | Lorain-Levi syndrome | Синдром Лорена | 1 |
| Q4420129 [CC | ] | Mauriac syndrome | Синдром Мориака | 1 |
| Q2165266 [CC | ] | Nelson syndrome | Синдром Нельсона | 1 |
| Q4420130 [CC | ] | Nobekur's syndrome | Синдром Нобекура | 1 |
| Q1543446 [CC | ] | Noonan syndrome | Синдром Нунан | 1 |
| Q959457 [CC | ] | syndrome of Inappropriate antidiuretic hormone secretion | Синдром Пархона | 1 |
| Q1276885 [CC | ] | Froelich syndrome | Синдром Пехкранца — Бабинского — Фрелиха | 1 |
| Q594013 [CC | ] | Prader–Willi syndrome | Синдром Прадера — Вилли | 1 |
| Q2037224 [CC | ] | partial androgen insensitivity syndrome | Синдром Рейфенштейна | 1 |
| Q604075 [CC | ] | multiple endocrine neoplasia type 2A | Синдром Сиппла | 1 |
| Q1770836 [CC | ] | Sotos syndrome | Синдром Сотоса | 1 |
| Q202849 [CC | ] | Turner syndrome | Синдром Шерешевского — Тёрнера | 1 |
| Q535876 [CC | ] | Sheehan's syndrome | Синдром Шихана | 1 |
| Q1418225 [CC | ] | autoimmune polyendocrine syndrome type 2 | Синдром Шмидта | 1 |
| Q219102 [CC | ] | Cushing's syndrome | Синдром гиперкортицизма | 1 |
| Q1179460 [CC | ] | Fanconi syndrome | Синдром де Тони — Дебре — Фанкони | 1 |
| Q512313 [CC | ] | androgen insensitivity syndrome | Синдром нечувствительности к андрогенам | 1 |
| Q500816 [CC | ] | polycystic ovary syndrome | Синдром поликистозных яичников | 1 |
| Q1467170 [CC | ] | Chronic Somogyi rebound | Синдром хронической передозировки инсулина | 1 |
| Q407166 [CC | ] | somatostatin | Соматостатин | 1 |
| Q1736456 [CC | ] | somatostatinoma | Соматостатинома | 1 |
| Q422137 [CC | ] | steroid hormone | Стероидные гормоны | 1 |
| Q441544 [CC | ] | TTG | ТТГ | 1 |
| Q1318776 [CC | ] | testosterone | Тестостерон | 1 |
| Q412228 [CC | ] | Thyroglobulin | Тиреоглобулин | 1 |
| Q11835644 [CC | ] | thyroiditis | Тиреоидит | 1 |
| Q16485 [CC | ] | De Quervain's thyroiditis | Тиреоидит де Кервена | 1 |
| Q4458080 [CC | ] | thyroid crisis | Тиреотоксический криз | 1 |
| Q188017 [CC | ] | L-tyrosine | Тирозин | 1 |
| Q2977746 [CC | ] | Toxic multinodular goitre | Токсическая аденома щитовидной железы | 1 |
| Q327362 [CC | ] | triiodothyronine | Трийодтиронин | 1 |
| Q409439 [CC | ] | tryptamine | Триптамин | 1 |
| Q424519 [CC | ] | thrombopoietin | Тромбопоэтин | 1 |
| Q53829 [CC | ] | thyroid nodule | Узловой зоб | 1 |
| Q536269 [CC | ] | phaeochromocytoma | Феохромоцитома | 1 |
| Q273499 [CC | ] | chemical synthesis | Химический синтез | 1 |
| Q60315441 [CC | ] | cholecystokinin | Холецистокинин | 1 |
| Q407172 [CC | ] | chorionic gonadotropin | Хорионический гонадотропин | 1 |
| Q4501724 [CC | ] | Chronic thyroiditis | Хронический тиреоидит | 1 |
| Q198654 [CC | ] | pineal gland | Шишковидное тело | 1 |
| Q407680 [CC | ] | icosanoid | Эйкозаноиды | 1 |
| Q1455531 [CC | ] | endemic goiter | Эндемический зоб | 1 |
| Q218706 [CC | ] | erythropoietin | Эритропоэтин | 1 |
| Q422416 [CC | ] | 17β-estradiol | Эстрадиол | 1 |
| Q409721 [CC | ] | estriol | Эстриол | 1 |
| Q414986 [CC | ] | estrone | Эстрон | 1 |
| Q415563 [CC | ] | ethinylestradiol | Этинилэстрадиол | 1 |
| Q80726 [CC | ] | allele | Allèle | 1 |
| Q1136569 [CC | ] | prenatal testing | Diagnostic prénatal | 1 |
| Q665092 [CC | ] | list of genetic disorders | Liste des maladies génétiques à gène identifié | 1 |
| Q96482784 [CC | ] | Pendred | Pendred | 1 |
| Q719602 [CC | ] | prevalence | Prévalence | 1 |
| Q101065 [CC | ] | puberty | Puberté | 1 |
| Q2823145 [CC | ] | achondrogenesis | Achondrogenesis | 1 |
| Q17010855 [CC | ] | achondrogenesis type IB | Achondrogenesis type 1B | 1 |
| Q937818 [CC | ] | acrodermatitis enteropathica | Acrodermatitis enteropathica | 1 |
| Q4690019 [CC | ] | African iron overload | African iron overload | 1 |
| Q4731121 [CC | ] | Allan-Herndon-Dudley syndrome | Allan–Herndon–Dudley syndrome | 1 |
| Q4216194 [CC | ] | arterial tortuosity syndrome | Arterial tortuosity syndrome | 1 |
| Q2870197 [CC | ] | atelosteogenesis type II | Atelosteogenesis, type II | 1 |
| Q1125675 [CC | ] | congenital disorder of glycosylation | Congenital disorder of glycosylation | 1 |
| Q5160439 [CC | ] | Congenital hypopituitarism | Congenital hypopituitarism | 1 |
| Q1472 [CC | ] | Crohn's disease | Crohn's disease | 1 |
| Q1149046 [CC | ] | cystinuria | Cystinuria | 1 |
| Q3335666 [CC | ] | diastrophic dysplasia | Diastrophic dysplasia | 1 |
| Q21503282 [CC | ] | episodic ataxia | Episodic ataxia | 1 |
| Q204335 [CC | ] | eponym | Eponym | 1 |
| Q417234 [CC | ] | Solute carrier family 40 member 1 | Ferroportin | 1 |
| Q1671489 [CC | ] | fructose malabsorption | Fructose malabsorption | 1 |
| Q1464888 [CC | ] | Fuchs' endothelial dystrophy | Fuchs' dystrophy | 1 |
| Q24722601 [CC | ] | glucose transporter, type 1 | GLUT1 | 1 |
| Q24722849 [CC | ] | glucose transporter, type 2 | GLUT2 | 1 |
| Q18031527 [CC | ] | SLC2A5 | GLUT5 | 1 |
| Q1053120 [CC | ] | Gitelman syndrome | Gitelman syndrome | 1 |
| Q5572341 [CC | ] | glucose-galactose malabsorption | Glucose-galactose malabsorption | 1 |
| Q200985 [CC | ] | Hartnup disease | Hartnup disease | 1 |
| Q2920572 [CC | ] | cranial trauma | Head injury | 1 |
| Q2298020 [CC | ] | hereditary elliptocytosis | Hereditary elliptocytosis | 1 |
| Q541244 [CC | ] | hereditary spherocytosis | Hereditary spherocytosis | 1 |
| Q11612732 [CC | ] | hyperinsulinemic hypoglycemia | Hyperinsulinemic hypoglycemia | 1 |
| Q3153671 [CC | ] | lysinuric protein intolerance | Lysinuric protein intolerance | 1 |
| Q1452604 [CC | ] | multiple epiphyseal dysplasia | Multiple epiphyseal dysplasia | 1 |
| Q9079046 [CC | ] | nonsyndromic deafness | Nonsyndromic deafness | 1 |
| Q1207967 [CC | ] | renal glycosuria | Renal glycosuria | 1 |
| Q18035831 [CC | ] | SLC17A3 | SLC17A3 | 1 |
| Q18046837 [CC | ] | SLC2A10 | SLC2A10 | 1 |
| Q1753883 [CC | ] | SNOMED CT | SNOMED CT | 1 |
| Q126265136 [CC | ] | SPATCCM | SPATCCM | 1 |
| Q3843807 [CC | ] | Salla disease | Salla disease | 1 |
| Q14905340 [CC | ] | SLC12A3 | Sodium-chloride symporter | 1 |
| Q1401099 [CC | ] | solute carrier family | Solute carrier family | 1 |
| Q712838 [CC | ] | thyroid function tests | Thyroid function tests | 1 |
| Q118455746 [CC | ] | authority control | Control de autoridades | 1 |
| Q21 [CC | ] | England | Inglaterra | 1 |
| Q8054 [CC | ] | protein | Proteína | 1 |
| Q2013 [CC | ] | Wikidata | Wikidata | 1 |
| Q7846 [CC | ] | 1896 | 1896 | 1 |
| Q2070 [CC | ] | 1996 | 1996 | 1 |
| Q183560 [CC | ] | intellectual disability | Kehitysvamma | 1 |
| Q11190 [CC | ] | medicine | Lääketiede | 1 |
| Q787488 [CC | ] | ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases | ICD10 Hoofdstuk IV | 1 |
| Q424972 [CC | ] | prednisone | Prednison | 1 |
| Q204127 [CC | ] | Struma | Struma | 1 |
| Q16644043 [CC | ] | diagnosis | Diagnosi | 1 |
| Q9647 [CC | ] | gland | Ghiandola | 1 |
| Q724965 [CC | ] | cochlear implant | Impianto cocleare | 1 |
| Q42406 [CC | ] | English people | Inglesi | 1 |
| Q7362 [CC | ] | ear | Orecchio | 1 |
| Q3808900 [CC | ] | sensitivity and specificity | Specificità | 1 |
| Q1995526 [CC | ] | traumatic brain injury | Trauma cranico | 1 |
| Q7565 [CC | ] | father | أب | 1 |
| Q12183115 [CC | ] | No label in en! | اضطراب (توضيح) | 1 |
| Q180686 [CC | ] | PubMed | ببمد | 1 |
| Q229883 [CC | ] | PubMed Central | ببمد سنترال | 1 |
| Q3279041 [CC | ] | vestibule of the ear | دهليز الأذن | 1 |
| Q12212008 [CC | ] | No label in en! | دوار (توضيح) | 1 |
| Q348996 [CC | ] | Head | رأس (توضيح) | 1 |
| Q160289 [CC | ] | hearing | سمع | 1 |
| Q276258 [CC | ] | childhood | طفولة | 1 |
| Q28923113 [CC | ] | No label in en! | قوقعة (توضيح) | 1 |
| Q12238782 [CC | ] | المجاز | مجاز (توضيح) | 1 |
| Q645858 [CC | ] | dietary supplement | مكمل غذائي | 1 |
| Q774740 [CC | ] | Bus | ناقلات (توضيح) | 1 |
| Q455338 [CC | ] | Unified Medical Language System | نظام اللغة الطبية الموحدة | 1 |
| Q25754 [CC | ] | bibcode | Bibcode | 1 |
| Q25554703 [CC | ] | No label in en! | Autosomno nasljeđivanje | 1 |
| Q1425030 [CC | ] | genetic carrier | Genetički nositelj | 1 |
| Q501898 [CC | ] | heterozygotes | Heterozigot | 1 |
| Q1071953 [CC | ] | medical genetics | Medicinska genetika | 1 |
| Q21115754 [CC | ] | Solute carrier family 16 member 1 | SLC16A1 | 1 |
| Q425149 [CC | ] | Solute carrier family 4 member 1 (Diego blood group) | SLC4A1 | 1 |
| Q10686316 [CC | ] | vertigo | Vrtoglavica | 1 |