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.
Q1996246 - hereditary lymphedema
Searching link targets on 8 Wikipedias...
| Item | Label [en] | Wikilabels | Link # |
|---|---|---|---|
Q241953 [CC |  ] | Online Mendelian Inheritance in Man | Online Mendelian Inheritance in Man | Héritage mendélien chez l'humain | الوراثة المندلية البشرية عبر الإنترنت | Herencia Mendeliana en el Hombre | OMIM | Mendelian Inheritance in Man | 7 |
| Q916398 [CC | ] | lymphedema | Linfedema | Lymphœdème | وذمة لمفية | Lymphödem | Lymphedema | 7 |
| Q305913 [CC | ] | eMedicine | EMedicine | إي ميديسين | 6 |
| Q1071953 [CC | ] | medical genetics | Genética médica | علم الوراثة الطبية | Di truyền học y khoa | Genetica clinica | Medical genetics | 6 |
| Q33057 [CC | ] | International Standard Book Number | ISBN | النظام القياسي الدولي لترقيم الكتب | International Standard Book Number | 5 |
| Q213103 [CC | ] | Diseases Database | Diseases Database | قاعدة بيانات الأمراض | 5 |
| Q76432 [CC | ] | Rudolf Virchow | Rudolf Virchow | رودلف فيرخوف | 4 |
| Q216211 [CC | ] | hypertrophy | Hipertrofia | Phì đại | Ipertrofia | Hypertrophy | 4 |
| Q712604 [CC | ] | lymphatic system | Sistema linfático | Hệ bạch huyết | Lymphatic system | 4 |
| Q7187 [CC | ] | gene | Gen | Gène | 3 |
| Q584211 [CC | ] | hydrocele | Hydrocèle | Idrocele | Hydrocele | 3 |
| Q930752 [CC | ] | medical specialty | اختصاص طبي | Especialidades médicas | Medical specialty | 3 |
| Q3832889 [CC | ] | Lymphangiectasia | توسع الأوعية اللمفية | Lymphangiektasie | Lymphangiectasia | 3 |
| Q7243149 [CC | ] | Primary lymphedema | وذمة لمفية أولية | Nonne-Milroy-Meige-Syndrom | Primary lymphedema | 3 |
| Q45127 [CC | ] | International Classification of Diseases, Tenth Revision (ICD-10) | ICD-10 | 3 |
| Q840741 [CC | ] | human chromosome 5 | Chromosome 5 humain | Chromosom 5 (Mensch) | 2 |
| Q1090224 [CC | ] | chylothorax | Chylothorax | 2 |
| Q116406 [CC | ] | autosomal dominant | Transmission autosomique dominante | Autosomal-dominanter Erbgang | 2 |
| Q1545572 [CC | ] | splenic infarction | احتشاء الطحال | Splenic infarction | 2 |
| Q152234 [CC | ] | edema | استسقاء (طب) | Edema | 2 |
| Q1476027 [CC | ] | lymphangitis | التهاب الأوعية اللمفية | Lymphangitis | 2 |
| Q1860 [CC | ] | English | اللغة الإنجليزية | Englische Sprache | 2 |
| Q737712 [CC | ] | asplenia | انعدام الطحال | Asplenia | 2 |
| Q1129121 [CC | ] | splenomegaly | تضخم الطحال | Splenomegaly | 2 |
| Q847726 [CC | ] | lymphadenopathy | تضخم العقد اللمفية | Lymphadenopathy | 2 |
| Q2834267 [CC | ] | polysplenia | تعدد الطحال | Polysplenia | 2 |
| Q4669672 [CC | ] | Abscess of thymus | خراجات الغدة التوتية | Abscess of thymus | 2 |
| Q9371 [CC | ] | spleen | طحال | Spleen | 2 |
| Q1129625 [CC | ] | accessory spleen | طحال إضافي | Accessory spleen | 2 |
| Q170758 [CC | ] | lymph node | عقدة لمفاوية | Lymph node | 2 |
| Q163987 [CC | ] | thymus | غدة زعترية | Thymus | 2 |
| Q7799652 [CC | ] | Thymus hyperplasia | فرط تنسج صعتري | Thymus hyperplasia | 2 |
| Q3843800 [CC | ] | chronic congestive splenomegaly | متلازمة بانتي | Banti's syndrome | 2 |
| Q525642 [CC | ] | DiGeorge syndrome | متلازمة دي جورج | DiGeorge syndrome | 2 |
| Q3508768 [CC | ] | Lymphedema–distichiasis syndrome | متلازمة وذمة ازدواجية الأهداب اللمفية | Lymphedema–distichiasis syndrome | 2 |
| Q12136 [CC | ] | disease | مرض | Malattia | 2 |
| Q1060827 [CC | ] | Kikuchi disease | مرض كيكوتشي | Kikuchi disease | 2 |
| Q6708237 [CC | ] | lymphatic system disease | مرض لمفاوي | Lymphatic disease | 2 |
| Q66683 [CC | ] | Who Named It? | من سمى هذا؟ | Who Named It? | 2 |
| Q909442 [CC | ] | Kyoto Encyclopedia of Genes and Genomes | موسوعة كيوتو للجينات والمجينات | KEGG | 2 |
| Q7799616 [CC | ] | thymic hypoplasia | نقص تنسج التوتة | Thymic hypoplasia | 2 |
| Q602528 [CC | ] | Henry Meige | هنري ميج | Henry Meige | 2 |
| Q7234336 [CC | ] | Postinflammatory lymphedema | وذمة لمفية بعد الالتهاب | Postinflammatory lymphedema | 2 |
| Q7443853 [CC | ] | Secondary lymphedema | وذمة لمفية ثانوية | Secondary lymphedema | 2 |
| Q4997016 [CC | ] | Bullous lymphedema | وذمة لمفية فقاعية | Bullous lymphedema | 2 |
| Q16964430 [CC | ] | Lymphedema praecox | وذمة لمفية مبكرة | Lymphedema praecox | 2 |
| Q5428694 [CC | ] | Factitial lymphedema | وذمة لمفية مفتعلة | Factitial lymphedema | 2 |
| Q11238641 [CC | ] | lymphatic vessel | وعاء لمفي | Lymphatic vessel | 2 |
| Q25670 [CC | ] | digital object identifier | Digital object identifier | 2 |
| Q17928864 [CC | ] | FLT4 | FLT4 | 2 |
| Q199897 [CC | ] | Medical Subject Headings | Medical Subject Headings | 2 |
| Q1515833 [CC | ] | Orphanet | Orphanet | 2 |
| Q200779 [CC | ] | genetic disease | Bệnh di truyền | Erbkrankheit | 2 |
| Q1075923 [CC | ] | cholestasis | Colestasi | Cholestase | 2 |
| Q3048291 [CC | ] | GeneReviews | GeneReviews | 2 |
| Q86848 [CC | ] | Max Nonne | Max Nonne | 2 |
| Q80726 [CC | ] | allele | Allèle | 1 |
| Q37748 [CC | ] | chromosome | Chromosome | 1 |
| Q217690 [CC | ] | incidence | Incidence (épidémiologie) | 1 |
| Q665092 [CC | ] | list of genetic disorders | Liste des maladies génétiques à gène identifié | 1 |
| Q1549382 [CC | ] | asymptomatic carrier | Porteur sain | 1 |
| Q516389 [CC | ] | penetrance | Pénétrance | 1 |
| Q7701 [CC | ] | 1863 | 1863 | 1 |
| Q7839 [CC | ] | 1892 | 1892 | 1 |
| Q815753 [CC | ] | filariasis | داء الخيطيات | 1 |
| Q1947302 [CC | ] | Castleman's disease | داء كاسلمان | 1 |
| Q12078 [CC | ] | cancer | سرطان | 1 |
| Q577 [CC | ] | year | سنة | 1 |
| Q28923178 [CC | ] | No label in en! | سير (توضيح) | 1 |
| Q180569 [CC | ] | tonsil | لوزة | 1 |
| Q455338 [CC | ] | Unified Medical Language System | نظام اللغة الطبية الموحدة | 1 |
| Q133805 [CC | ] | epidemiology | وبائيات | 1 |
| Q14067712 [CC | ] | International Classification of Diseases, Ninth Revision (ICD-9) | CID-9 | 1 |
| Q189146 [CC | ] | cell-mediated immunity | Imunidade mediada por célula | 1 |
| Q9639 [CC | ] | intestine | Intestino | 1 |
| Q715347 [CC | ] | lymphocyte | Linfócito | 1 |
| Q27881569 [CC | ] | list of ICD-10 codes | Lista de códigos da CID-10 | 1 |
| Q557919 [CC | ] | MedlinePlus | MedlinePlus | 1 |
| Q1492 [CC | ] | Barcelona | Barcelona | 1 |
| Q5737131 [CC | ] | ICD-9-CM | CIE-9-MC | 1 |
| Q118455746 [CC | ] | authority control | Control de autoridades | 1 |
| Q45762085 [CC | ] | Círculo de Lectores, S.A. | Círculo de Lectores | 1 |
| Q3311537 [CC | ] | hereditary disorder | Enfermedad hereditaria | 1 |
| Q929833 [CC | ] | rare disease | Enfermedad rara | 1 |
| Q166231 [CC | ] | infection | Infección | 1 |
| Q12171 [CC | ] | menstruation | Menstruación | 1 |
| Q40397 [CC | ] | tissue | Tejido (biología) | 1 |
| Q2013 [CC | ] | Wikidata | Wikidata | 1 |
| Q661015 [CC | ] | achalasia | Acalasia | 1 |
| Q340548 [CC | ] | achlorhydria | Acloridria | 1 |
| Q539491 [CC | ] | angiodysplasia | Angiodisplasia | 1 |
| Q527465 [CC | ] | antibiogram | Antibiogramma | 1 |
| Q9649 [CC | ] | human digestive system | Apparato digerente | 1 |
| Q7895 [CC | ] | reproductive system | Apparato genitale | 1 |
| Q9656 [CC | ] | appendix | Appendice vermiforme | 1 |
| Q121041 [CC | ] | appendicitis | Appendicite | 1 |
| Q2465231 [CC | ] | anal canal | Canale anale | 1 |
| Q11088 [CC | ] | celiac disease | Celiachia | 1 |
| Q876887 [CC | ] | cellulitis | Cellulite (infezione) | 1 |
| Q147778 [CC | ] | liver cirrhosis | Cirrosi epatica | 1 |
| Q64386 [CC | ] | gallbladder | Cistifellea | 1 |
| Q1058608 [CC | ] | primary sclerosing cholangitis | Colangite sclerosante primitiva | 1 |
| Q2105535 [CC | ] | porcelain gallbladder | Colecisti a porcellana | 1 |
| Q376666 [CC | ] | cholecystitis | Colecistite | 1 |
| Q1263617 [CC | ] | common bile duct | Coledoco | 1 |
| Q272714 [CC | ] | gallstone | Colelitiasi | 1 |
| Q1075909 [CC | ] | strawberry gallbladder | Colesterolosi della colecisti | 1 |
| Q2453464 [CC | ] | colitis | Colite | 1 |
| Q450470 [CC | ] | collagenous colitis | Colite collagenosica | 1 |
| Q1532338 [CC | ] | ischemic colitis | Colite ischemica | 1 |
| Q6708258 [CC | ] | lymphocytic colitis | Colite linfocitica | 1 |
| Q2058941 [CC | ] | microscopic colitis | Colite microscopica | 1 |
| Q574905 [CC | ] | Clostridioides difficile colitis | Colite pseudomembranosa | 1 |
| Q5982337 [CC | ] | colon | Colon | 1 |
| Q1477327 [CC | ] | Fecal impaction | Coprostasi | 1 |
| Q40878 [CC | ] | diarrhea | Diarrea | 1 |
| Q574891 [CC | ] | antibiotic-associated diarrhea | Diarrea associata agli antibiotici | 1 |
| Q44602 [CC | ] | fasting | Digiuno | 1 |
| Q653971 [CC | ] | indigestion | Dispepsia | 1 |
| Q5508825 [CC | ] | functional gastrointestinal disorder | Disturbi funzionali gastrointestinali | 1 |
| Q1066061 [CC | ] | diverticulitis | Diverticolite | 1 |
| Q189638 [CC | ] | Zenker's diverticulum | Diverticolo di Zenker | 1 |
| Q278158 [CC | ] | diverticulosis | Diverticolosi | 1 |
| Q3454555 [CC | ] | dominance | Dominanza (genetica) | 1 |
| Q1266418 [CC | ] | duodenitis | Duodenite | 1 |
| Q134955 [CC | ] | duodenum | Duodeno | 1 |
| Q1570161 [CC | ] | hematemesis | Ematemesi | 1 |
| Q1642049 [CC | ] | hematochezia | Ematochezia | 1 |
| Q3144934 [CC | ] | HFE hereditary haemochromatosis | Emocromatosi ereditaria | 1 |
| Q1510899 [CC | ] | hemoperitoneum | Emoperitoneo | 1 |
| Q2915863 [CC | ] | lower gastrointestinal bleeding | Emorragia digestiva inferiore | 1 |
| Q1495657 [CC | ] | gastrointestinal bleeding | Emorragia gastrointestinale | 1 |
| Q642548 [CC | ] | hepatic encephalopathy | Encefalopatia epatica | 1 |
| Q854353 [CC | ] | enteritis | Enterite | 1 |
| Q3055368 [CC | ] | enterocolitis | Enterocolite | 1 |
| Q10859678 [CC | ] | necrotizing enterocolitis | Enterocolite necrotizzante | 1 |
| Q131742 [CC | ] | hepatitis | Epatite | 1 |
| Q3144986 [CC | ] | alcoholic hepatitis | Epatite alcolica | 1 |
| Q786844 [CC | ] | autoimmune hepatitis | Epatite autoimmune | 1 |
| Q1983841 [CC | ] | viral hepatitis | Epatite virale | 1 |
| Q929737 [CC | ] | liver disease | Epatopatia | 1 |
| Q558404 [CC | ] | alcoholic liver disease | Epatopatia alcolica | 1 |
| Q2334877 [CC | ] | nutmeg liver | Epatopatia congestizia | 1 |
| Q133076 [CC | ] | hernia | Ernia | 1 |
| Q3732357 [CC | ] | No label in en! | Ernia di Richter | 1 |
| Q2066669 [CC | ] | Spigelian hernia | Ernia di Spigelio | 1 |
| Q2119430 [CC | ] | diaphragmatic hernia | Ernia diaframmatica | 1 |
| Q727153 [CC | ] | hiatus hernia | Ernia iatale | 1 |
| Q298230 [CC | ] | esophagitis | Esofagite | 1 |
| Q2057356 [CC | ] | eosinophilic esophagitis | Esofagite eosinofila | 1 |
| Q2849596 [CC | ] | Herpes esophagitis | Esofagite erpetica | 1 |
| Q173710 [CC | ] | esophagus | Esofago | 1 |
| Q808892 [CC | ] | Barrett's esophagus | Esofago di Barrett | 1 |
| Q183130 [CC | ] | gastritis | Gastrite | 1 |
| Q1826391 [CC | ] | atrophic gastritis | Gastrite atrofica | 1 |
| Q975705 [CC | ] | gastric mucosal hypertrophy | Gastrite ipertrofica gigante | 1 |
| Q156103 [CC | ] | gastroenteritis | Gastroenterite | 1 |
| Q1130192 [CC | ] | Basuritis | Gastroenterocolite | 1 |
| Q943897 [CC | ] | gastroparesis | Gastroparesi | 1 |
| Q3796380 [CC | ] | ileitis | Ileite | 1 |
| Q233345 [CC | ] | ileum | Ileo (intestino) | 1 |
| Q970208 [CC | ] | liver failure | Insufficienza epatica | 1 |
| Q1192530 [CC | ] | acute liver failure | Insufficienza epatica acuta | 1 |
| Q11083 [CC | ] | large intestine | Intestino crasso | 1 |
| Q11090 [CC | ] | small intestine | Intestino tenue | 1 |
| Q1424612 [CC | ] | intussusception | Invaginazione | 1 |
| Q124604 [CC | ] | portal hypertension | Ipertensione portale | 1 |
| Q221463 [CC | ] | mesenteric ischemia | Ischemia mesenterica | 1 |
| Q1632678 [CC | ] | Mallory–Weiss syndrome | Lacerazione di Mallory-Weiss | 1 |
| Q2633160 [CC | ] | incisional hernia | Laparocele | 1 |
| Q3832892 [CC | ] | No label in en! | Linfangiografia | 1 |
| Q56325544 [CC | ] | No label in en! | Linfoscintigrafia degli arti | 1 |
| Q1442923 [CC | ] | malabsorption | Malassorbimento | 1 |
| Q367616 [CC | ] | Laryngopharyngeal reflux | Malattia da reflusso faringo-laringeo | 1 |
| Q223591 [CC | ] | gastroesophageal reflux disease | Malattia da reflusso gastroesofageo | 1 |
| Q1472 [CC | ] | Crohn's disease | Malattia di Crohn | 1 |
| Q653078 [CC | ] | Whipple disease | Malattia di Whipple | 1 |
| Q117121 [CC | ] | Wilson disease | Malattia di Wilson | 1 |
| Q5731687 [CC | ] | hepatic veno-occlusive disease | Malattia veno occlusiva epatica | 1 |
| Q917447 [CC | ] | inflammatory bowel diseases | Malattie infiammatorie croniche intestinali | 1 |
| Q1754226 [CC | ] | megacolon | Megacolon | 1 |
| Q588321 [CC | ] | toxic megacolon | Megacolon tossico | 1 |
| Q1163908 [CC | ] | melena | Melena | 1 |
| Q6849688 [CC | ] | contrast agent | Mezzo di contrasto | 1 |
| Q2082879 [CC | ] | PubMed ID | PMID | 1 |
| Q9618 [CC | ] | pancreas | Pancreas | 1 |
| Q1527888 [CC | ] | pancreatitis | Pancreatite | 1 |
| Q854573 [CC | ] | acute pancreatitis | Pancreatite acuta | 1 |
| Q1996053 [CC | ] | chronic pancreatitis | Pancreatite cronica | 1 |
| Q2068039 [CC | ] | peliosis hepatis | Peliosi epatica | 1 |
| Q472052 [CC | ] | dyskinesia of esophagus | Peristalsi esofagea sintomatica | 1 |
| Q9629 [CC | ] | peritoneum | Peritoneo | 1 |
| Q223102 [CC | ] | peritonitis | Peritonite | 1 |
| Q3128789 [CC | ] | Spontaneous bacterial peritonitis | Peritonite batterica spontanea | 1 |
| Q5609817 [CC | ] | tinea pedis | Piede d'atleta | 1 |
| Q163469 [CC | ] | pneumoperitoneum | Pneumoperitoneo | 1 |
| Q2632078 [CC | ] | proctalgia fugax | Proctalgia fugace | 1 |
| Q941770 [CC | ] | proctitis | Proctite | 1 |
| Q2062483 [CC | ] | rectal prolapse | Prolasso rettale | 1 |
| Q1633590 [CC | ] | pruritus ani | Prurito anale | 1 |
| Q3924862 [CC | ] | intestinal pseudo-obstruction | Pseudo-ostruzione intestinale | 1 |
| Q689496 [CC | ] | pancreatic pseudocyst | Pseudocisti pancreatica | 1 |
| Q180686 [CC | ] | PubMed | PubMed | 1 |
| Q484797 [CC | ] | anal fissure | Ragade anale | 1 |
| Q158716 [CC | ] | rectum | Retto | 1 |
| Q1477 [CC | ] | ulcerative colitis | Rettocolite ulcerosa | 1 |
| Q3422583 [CC | ] | rectorrhagia | Rettorragia | 1 |
| Q209402 [CC | ] | nuclear magnetic resonance | Risonanza magnetica nucleare | 1 |
| Q239848 [CC | ] | dumping syndrome | Sindrome da dumping | 1 |
| Q1271831 [CC | ] | small intestinal bacterial overgrowth | Sindrome da iperproliferazione batterica | 1 |
| Q3961657 [CC | ] | anismus | Sindrome del pubo-rettale | 1 |
| Q662272 [CC | ] | short bowel syndrome | Sindrome dell'intestino corto | 1 |
| Q838966 [CC | ] | irritable bowel syndrome | Sindrome dell'intestino irritabile | 1 |
| Q535425 [CC | ] | Boerhaave syndrome | Sindrome di Boerhaave | 1 |
| Q183098 [CC | ] | hepatic vein thrombosis | Sindrome di Budd-Chiari | 1 |
| Q212726 [CC | ] | Mirizzi's syndrome | Sindrome di Mirizzi | 1 |
| Q1464904 [CC | ] | Ogilvie syndrome | Sindrome di Ogilvie | 1 |
| Q247131 [CC | ] | hepatorenal syndrome | Sindrome epatorenale | 1 |
| Q912766 [CC | ] | postcholecystectomy syndrome | Sindrome post-colecistectomia | 1 |
| Q851111 [CC | ] | bile ducts | Sistema biliare | 1 |
| Q1224503 [CC | ] | diffuse esophageal spasm | Spasmo esofageo diffuso | 1 |
| Q585911 [CC | ] | tropical sprue | Sprue tropicale | 1 |
| Q1549428 [CC | ] | steatorrhea | Steatorrea | 1 |
| Q6058862 [CC | ] | fatty liver disease | Steatosi epatica | 1 |
| Q1027995 [CC | ] | pyloric stenosis | Stenosi ipertrofica del piloro | 1 |
| Q178436 [CC | ] | constipation | Stitichezza | 1 |
| Q1029907 [CC | ] | stomach | Stomaco | 1 |
| Q32566 [CC | ] | computed tomography | Tomografia computerizzata | 1 |
| Q5196200 [CC | ] | Cushing ulcer | Ulcera di Cushing | 1 |
| Q172941 [CC | ] | peptic ulcer disease | Ulcera peptica | 1 |
| Q388388 [CC | ] | intestinal volvulus | Volvolo | 1 |
| Q369668 [CC | ] | William Osler | William Osler | 1 |
| Q1233688 [CC | ] | DocCheck | DocCheck | 1 |
| Q101991 [CC | ] | inflammation | Entzündung | 1 |
| Q34581 [CC | ] | parturition | Geburt | 1 |
| Q106227 [CC | ] | locus | Genlocus | 1 |
| Q11180 [CC | ] | internal medicine | Innere Medizin | 1 |
| Q14640281 [CC | ] | Journal of Medical Genetics | Journal of Medical Genetics | 1 |
| Q745049 [CC | ] | compression stockings | Kompressionsstrumpf | 1 |
| Q397 [CC | ] | Latin | Latein | 1 |
| Q42918 [CC | ] | mutation | Mutation | 1 |
| Q83042 [CC | ] | neurology | Neurologie | 1 |
| Q101065 [CC | ] | puberty | Pubertät | 1 |
| Q42106 [CC | ] | synonym | Synonym | 1 |
| Q21115319 [CC | ] | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | ATP2A2 | 1 |
| Q4672539 [CC | ] | accessory nail of the fifth toe | Accessory nail of the fifth toe | 1 |
| Q4675781 [CC | ] | punctate palmoplantar keratoderma type III | Acrokeratoelastoidosis of Costa | 1 |
| Q2619091 [CC | ] | angiosarcoma | Angiosarcoma | 1 |
| Q1424491 [CC | ] | aplasia cutis congenita | Aplasia cutis congenita | 1 |
| Q193889 [CC | ] | ascites | Ascites | 1 |
| Q772022 [CC | ] | asplenia with cardiovascular anomalies | Asplenia with cardiovascular anomalies | 1 |
| Q4865826 [CC | ] | Bart-Pumphrey syndrome | Bart–Pumphrey syndrome | 1 |
| Q3513591 [CC | ] | birthmark | Birthmark | 1 |
| Q4973829 [CC | ] | bronchogenic cyst | Bronchogenic cyst | 1 |
| Q8075299 [CC | ] | CHIME syndrome | CHIME syndrome | 1 |
| Q24776048 [CC | ] | cadherin | Cadherin | 1 |
| Q5026799 [CC | ] | Camisa disease | Camisa disease | 1 |
| Q2072821 [CC | ] | capillary hemangioma | Capillary hemangioma | 1 |
| Q14902080 [CC | ] | CTSC | Cathepsin C | 1 |
| Q5055067 [CC | ] | Cavernous venous malformation | Cavernous venous malformation | 1 |
| Q5135822 [CC | ] | Clouston syndrome | Clouston's hidrotic ectodermal dysplasia | 1 |
| Q5160411 [CC | ] | Congenital cartilaginous rest of the neck | Congenital cartilaginous rest of the neck | 1 |
| Q5160436 [CC | ] | Congenital hypertrophy of the lateral fold of the hallux | Congenital hypertrophy of the lateral fold of the hallux | 1 |
| Q3731836 [CC | ] | congenital ichthyosiform erythroderma | Congenital ichthyosiform erythroderma | 1 |
| Q5160444 [CC | ] | Congenital lip pit | Congenital lip pit | 1 |
| Q5160443 [CC | ] | congenital malformations of the dermatoglyphs | Congenital malformations of the dermatoglyphs | 1 |
| Q5160449 [CC | ] | congenital smooth muscle hamartoma | Congenital smooth muscle hamartoma | 1 |
| Q1779300 [CC | ] | connective tissue disease | Connective tissue disease | 1 |
| Q423489 [CC | ] | connexins | Connexin | 1 |
| Q5171588 [CC | ] | Corneodermatoosseous syndrome | Corneodermatoosseous syndrome | 1 |
| Q1136492 [CC | ] | Costello syndrome | Costello syndrome | 1 |
| Q2735907 [CC | ] | cutis laxa | Cutis laxa | 1 |
| Q5201213 [CC | ] | Cystic lymphatic malformation | Cystic lymphatic malformation | 1 |
| Q580506 [CC | ] | keratosis follicularis | Darier's disease | 1 |
| Q5262702 [CC | ] | dermatopathia pigmentosa reticularis | Dermatopathia pigmentosa reticularis | 1 |
| Q1200267 [CC | ] | dermoid cyst | Dermoid cyst | 1 |
| Q5264821 [CC | ] | Desmoplakin | Desmoplakin | 1 |
| Q5277223 [CC | ] | dime museum | Dime museum | 1 |
| Q5290299 [CC | ] | dominant dystrophic epidermolysis bullosa | Dominant dystrophic epidermolysis bullosa | 1 |
| Q3709312 [CC | ] | dyskeratosis congenita | Dyskeratosis congenita | 1 |
| Q5322931 [CC | ] | EEM syndrome | EEM syndrome | 1 |
| Q1323713 [CC | ] | ectodermal dysplasia | Ectodermal dysplasia | 1 |
| Q5334295 [CC | ] | ectopic thymus | Ectopic thymus | 1 |
| Q1141499 [CC | ] | Ehlers-Danlos syndrome | Ehlers–Danlos syndrome | 1 |
| Q259817 [CC | ] | elastic fiber | Elastic fiber | 1 |
| Q1346023 [CC | ] | encephalocele | Encephalocele | 1 |
| Q3055380 [CC | ] | intestinal disease | Enteropathy | 1 |
| Q923020 [CC | ] | epidermolysis bullosa | Epidermolysis bullosa | 1 |
| Q3589131 [CC | ] | epidermolysis bullosa dystrophica | Epidermolysis bullosa dystrophica | 1 |
| Q5382846 [CC | ] | epidermolysis bullosa herpetiformis | Epidermolysis bullosa herpetiformis | 1 |
| Q3124960 [CC | ] | epidermolysis bullosa simplex | Epidermolysis bullosa simplex | 1 |
| Q5382847 [CC | ] | epidermolysis bullosa simplex of Ogna | Epidermolysis bullosa simplex of Ogna | 1 |
| Q5382848 [CC | ] | epidermolysis bullosa simplex with mottled pigmentation | Epidermolysis bullosa simplex with mottled pigmentation | 1 |
| Q5382849 [CC | ] | epidermolysis bullosa simplex with muscular dystrophy | Epidermolysis bullosa simplex with muscular dystrophy | 1 |
| Q3801491 [CC | ] | epidermolytic hyperkeratosis | Epidermolytic hyperkeratosis | 1 |
| Q5396475 [CC | ] | Erythrokeratodermia | Erythrokeratodermia | 1 |
| Q3591493 [CC | ] | erythrokeratodermia variabilis | Erythrokeratodermia variabilis | 1 |
| Q14905606 [CC | ] | FOXC2 | FOXC2 | 1 |
| Q21290101 [CC | ] | Fanny Mills | Fanny Mills | 1 |
| Q5463847 [CC | ] | focal dermal hypoplasia | Focal dermal hypoplasia | 1 |
| Q5463857 [CC | ] | Focal palmoplantar and gingival keratosis | Focal palmoplantar and gingival keratosis | 1 |
| Q5532470 [CC | ] | generalized epidermolysis bullosa simplex | Generalized epidermolysis bullosa simplex | 1 |
| Q5532491 [CC | ] | Generalized lymphadenopathy | Generalized lymphadenopathy | 1 |
| Q666075 [CC | ] | genodermatosis | Genodermatosis | 1 |
| Q5552374 [CC | ] | gerodermia osteodysplastica | Gerodermia osteodysplastica | 1 |
| Q863861 [CC | ] | Hailey-Hailey disease | Hailey–Hailey disease | 1 |
| Q5639341 [CC | ] | Haim–Munk syndrome | Haim–Munk syndrome | 1 |
| Q266421 [CC | ] | autosomal recessive congenital ichthyosis | Harlequin-type ichthyosis | 1 |
| Q940210 [CC | ] | ankyloblepharon-ectodermal defects-cleft lip/palate syndrome | Hay–Wells syndrome | 1 |
| Q5921848 [CC | ] | Howel–Evans syndrome | Howel–Evans syndrome | 1 |
| Q1640998 [CC | ] | hyperkeratosis | Hyperkeratosis | 1 |
| Q1077955 [CC | ] | hypohidrotic ectodermal dysplasia | Hypohidrotic ectodermal dysplasia | 1 |
| Q5962435 [CC | ] | Hystrix-like ichthyosis–deafness syndrome | Hystrix-like ichthyosis–deafness syndrome | 1 |
| Q55695727 [CC | ] | ICD-11 | ICD-11 | 1 |
| Q5986438 [CC | ] | ichthyosis bullosa of Siemens | Ichthyosis bullosa of Siemens | 1 |
| Q5986448 [CC | ] | Ichthyosis hystrix | Ichthyosis hystrix | 1 |
| Q5986443 [CC | ] | Ichthyosis linearis circumflexa | Ichthyosis linearis circumflexa | 1 |
| Q5986451 [CC | ] | Ichthyosis prematurity syndrome | Ichthyosis prematurity syndrome | 1 |
| Q3765145 [CC | ] | ichthyosis vulgaris | Ichthyosis vulgaris | 1 |
| Q1059 [CC | ] | immune system | Immune system | 1 |
| Q1214385 [CC | ] | integument | Integument | 1 |
| Q6058489 [CC | ] | Intranodal palisaded myofibroblastoma | Intranodal palisaded myofibroblastoma | 1 |
| Q3726862 [CC | ] | junctional epidermolysis bullosa | Junctional epidermolysis bullosa (medicine) | 1 |
| Q3589130 [CC | ] | Junctional epidermolysis bullosa, Herlitz type | Junctional epidermolysis bullosa gravis | 1 |
| Q6311812 [CC | ] | junctional epidermolysis bullosa with pyloric atresia | Junctional epidermolysis bullosa with pyloric atresia | 1 |
| Q4219511 [CC | ] | Keratin disease | Keratin disease | 1 |
| Q1345746 [CC | ] | keratitis–ichthyosis–deafness syndrome | Keratitis–ichthyosis–deafness syndrome | 1 |
| Q1976193 [CC | ] | keratolytic winter erythema | Keratolytic winter erythema | 1 |
| Q6393653 [CC | ] | keratosis follicularis spinulosa decalvans | Keratosis follicularis spinulosa decalvans | 1 |
| Q6393657 [CC | ] | Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome | Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome | 1 |
| Q1637035 [CC | ] | keratosis pilaris | Keratosis pilaris | 1 |
| Q3548166 [CC | ] | keratosis pilaris atrophicans faciei | Keratosis pilaris atrophicans faciei | 1 |
| Q6393663 [CC | ] | Keratosis punctata of the palmar creases | Keratosis punctata of the palmar creases | 1 |
| Q1741965 [CC | ] | Kindler syndrome | Kindler syndrome | 1 |
| Q3804556 [CC | ] | lamellar ichthyosis | Lamellar ichthyosis | 1 |
| Q6520907 [CC | ] | Lelis syndrome | Lelis syndrome | 1 |
| Q1204354 [CC | ] | list of ICD-9 codes | List of ICD-9 codes | 1 |
| Q6664623 [CC | ] | localized epidermolysis bullosa simplex | Localized epidermolysis bullosa simplex | 1 |
| Q3913024 [CC | ] | lymphangiosarcoma | Lymphangiosarcoma | 1 |
| Q112670 [CC | ] | mastocytosis | Mastocytosis | 1 |
| Q6806134 [CC | ] | Median raphe cyst | Median raphe cyst | 1 |
| Q6809999 [CC | ] | Meige lymphedema | Meige disease | 1 |
| Q16938399 [CC | ] | melanotic neuroectodermal tumor | Melanotic neuroectodermal tumor of infancy | 1 |
| Q4352925 [CC | ] | Mal de Meleda | Meleda disease | 1 |
| Q1072716 [CC | ] | Mongolian spot | Mongolian spot | 1 |
| Q6966577 [CC | ] | Nasal glioma | Nasal glioma | 1 |
| Q6967228 [CC | ] | Nasolacrimal duct cyst | Nasolacrimal duct cyst | 1 |
| Q1332565 [CC | ] | Naxos disease | Naxos syndrome | 1 |
| Q9390284 [CC | ] | Netherton syndrome | Netherton syndrome | 1 |
| Q692077 [CC | ] | nevus | Nevus | 1 |
| Q1419862 [CC | ] | stork bite | Nevus flammeus nuchae | 1 |
| Q7088441 [CC | ] | Olmsted syndrome | Olmsted syndrome | 1 |
| Q7090704 [CC | ] | Omphalomesenteric duct cyst | Omphalomesenteric duct cyst | 1 |
| Q3360152 [CC | ] | pachyonychia congenita | Pachyonychia congenita | 1 |
| Q7122179 [CC | ] | Pachyonychia congenita type I | Pachyonychia congenita type I | 1 |
| Q7122180 [CC | ] | Pachyonychia congenita type II | Pachyonychia congenita type II | 1 |
| Q7128426 [CC | ] | palmoplantar keratosis | Palmoplantar keratoderma | 1 |
| Q2050791 [CC | ] | Papillon-Lefevre disease | Papillon–Lefèvre syndrome | 1 |
| Q21139990 [CC | ] | junction plakoglobin | Plakoglobin | 1 |
| Q1587881 [CC | ] | popliteal pterygium syndrome | Popliteal pterygium syndrome | 1 |
| Q1409611 [CC | ] | port-wine stain | Port-wine stain | 1 |
| Q1052391 [CC | ] | inherited pseudoxanthoma elasticum | Pseudoxanthoma elasticum | 1 |
| Q7294259 [CC | ] | Rapidly involuting congenital hemangioma | Rapidly involuting congenital hemangioma | 1 |
| Q7294342 [CC | ] | Rapp-Hodgkin syndrome | Rapp–Hodgkin syndrome | 1 |
| Q7302398 [CC | ] | recessive dystrophic epidermolysis bullosa | Recessive dystrophic epidermolysis bullosa | 1 |
| Q7368611 [CC | ] | Rosenthal–Kloepfer syndrome | Rosenthal–Kloepfer syndrome | 1 |
| Q7433355 [CC | ] | Schöpf–Schulz–Passarge syndrome | Schöpf–Schulz–Passarge syndrome | 1 |
| Q7434145 [CC | ] | Scleroatrophic syndrome of Huriez | Scleroatrophic syndrome of Huriez | 1 |
| Q9378133 [CC | ] | Sinus pericranii | Sinus pericranii | 1 |
| Q2291208 [CC | ] | Sjogren-Larsson syndrome | Sjögren–Larsson syndrome | 1 |
| Q7535383 [CC | ] | Skin dimple | Skin dimple | 1 |
| Q7535394 [CC | ] | Skin fragility syndrome | Skin fragility syndrome | 1 |
| Q7578547 [CC | ] | splenic tumor | Splenic tumor | 1 |
| Q7799620 [CC | ] | thymic carcinoma | Thymic carcinoma | 1 |
| Q1429863 [CC | ] | thymoma | Thymoma | 1 |
| Q7484623 [CC | ] | tyrosinemia type II | Tyrosinemia type II | 1 |
| Q3886247 [CC | ] | urticaria pigmentosa | Urticaria pigmentosa | 1 |
| Q2033532 [CC | ] | Van der Woude syndrome | Van der Woude syndrome | 1 |
| Q7939442 [CC | ] | Vohwinkel syndrome | Vohwinkel syndrome | 1 |
| Q7961531 [CC | ] | Waldmann disease | Waldmann disease | 1 |
| Q7967227 [CC | ] | Wandering spleen | Wandering spleen | 1 |
| Q3804555 [CC | ] | X-linked ichthyosis | X-linked ichthyosis | 1 |