English Wikipedia @ Freddythechick:WikiProject Medicine/The ICD-11 coding challenge/3200–3299

From English Wikipedia @ Freddythechick

This is page 33 / 67 of the ICD-11 coding challenge.

The data below was generated from Special:WhatLinksHere/Template:Medical resources.

Check as many of these articles as you can and, if needed, fill in the missing ICD-11 code(s)!

Find the right codes here:

# Article Done?
3200 Rhythmic movement disorder User:Manifestation/Not checked
3201 Esophageal candidiasis User:Manifestation/Not checked
3202 Dientamoebiasis User:Manifestation/Not checked
3203 Acanthamoeba keratitis User:Manifestation/Not checked
3204 Aggressive fibromatosis User:Manifestation/Not checked
3205 Burning mouth syndrome User:Manifestation/Not checked
3206 Pituitary apoplexy User:Manifestation/Not checked
3207 Uterine prolapse User:Manifestation/Not checked
3208 Splenic infarction User:Manifestation/Not checked
3209 Laurence–Moon syndrome User:Manifestation/Not checked
3210 Ménétrier's disease User:Manifestation/Not checked
3211 Dentin hypersensitivity User:Manifestation/Not checked
3212 Vascular disease User:Manifestation/Not checked
3213 Robinow syndrome User:Manifestation/Not checked
3214 Dercum's disease User:Manifestation/Not checked
3215 Monosomy 9p User:Manifestation/Not checked
3216 Oculocerebrorenal syndrome User:Manifestation/Not checked
3217 Adiposogenital dystrophy User:Manifestation/Not checked
3218 Hypocholesterolemia User:Manifestation/Not checked
3219 Lucey–Driscoll syndrome User:Manifestation/Not checked
3220 Xanthochromia User:Manifestation/Not checked
3221 Dirofilariasis User:Manifestation/Not checked
3222 Distal trisomy 10q User:Manifestation/Not checked
3223 Larsen syndrome User:Manifestation/Not checked
3224 Autonomic dysreflexia User:Manifestation/Not checked
3225 2-Methylbutyryl-CoA dehydrogenase deficiency User:Manifestation/Not checked
3226 Epidermolysis bullosa simplex User:Manifestation/Not checked
3227 Baritosis User:Manifestation/Not checked
3228 Muscle atrophy User:Manifestation/Not checked
3229 Beta thalassemia User:Manifestation/Not checked
3230 Halal syndrome User:Manifestation/Not checked
3231 Hypoglossia User:Manifestation/Not checked
3232 HEC syndrome User:Manifestation/Not checked
3233 Endocardial fibroelastosis User:Manifestation/Not checked
3234 Histidinemia User:Manifestation/Not checked
3235 Idiopathic CD4+ lymphocytopenia User:Manifestation/Not checked
3236 Pancreatic disease User:Manifestation/Not checked
3237 Circadian rhythm sleep disorder User:Manifestation/Not checked
3238 Hailey–Hailey disease User:Manifestation/Not checked
3239 Asplenia with cardiovascular anomalies User:Manifestation/Not checked
3240 Precordial catch syndrome User:Manifestation/Not checked
3241 Chordoma User:Manifestation/Not checked
3242 Pallister–Killian syndrome User:Manifestation/Not checked
3243 Dolichocephaly User:Manifestation/Not checked
3244 Impaired fasting glucose User:Manifestation/Not checked
3245 Fungal keratitis User:Manifestation/Not checked
3246 Succinic semialdehyde dehydrogenase deficiency User:Manifestation/Not checked
3247 Torus palatinus User:Manifestation/Not checked
3248 Calciphylaxis User:Manifestation/Not checked
3249 Prurigo nodularis User:Manifestation/Not checked
3250 Cavernous sinus thrombosis User:Manifestation/Not checked
3251 Carotid artery dissection User:Manifestation/Not checked
3252 ATR-X syndrome User:Manifestation/Not checked
3253 AREDYLD syndrome User:Manifestation/Not checked
3254 Abruzzo–Erickson syndrome User:Manifestation/Not checked
3255 Holt–Oram syndrome User:Manifestation/Not checked
3256 Shwartzman phenomenon User:Manifestation/Not checked
3257 Acrodynia User:Manifestation/Not checked
3258 Alström syndrome User:Manifestation/Not checked
3259 Autosomal dominant hypophosphatemic rickets User:Manifestation/Not checked
3260 Gender dysphoria in children User:Manifestation/Not checked
3261 Ego-dystonic sexual orientation User:Manifestation/Not checked
3262 N-Acetylglutamate synthase deficiency User:Manifestation/Not checked
3263 Sprengel's deformity User:Manifestation/Not checked
3264 Hypercalciuria User:Manifestation/Not checked
3265 XXXXY syndrome User:Manifestation/Not checked
3266 Stenosis of uterine cervix User:Manifestation/Not checked
3267 DNA repair-deficiency disorder User:Manifestation/Not checked
3268 Pseudohyperaldosteronism User:Manifestation/Not checked
3269 Brodie abscess User:Manifestation/Not checked
3270 Iridocorneal endothelial syndrome User:Manifestation/Not checked
3271 Hypobetalipoproteinemia User:Manifestation/Not checked
3272 Verrucous carcinoma User:Manifestation/Not checked
3273 Hyperhomocysteinemia User:Manifestation/Not checked
3274 Retinitis User:Manifestation/Not checked
3275 Toxic and nutritional optic neuropathy User:Manifestation/Not checked
3276 Ascending cholangitis User:Manifestation/Not checked
3277 Lentigo simplex User:Manifestation/Not checked
3278 Adams–Stokes syndrome User:Manifestation/Not checked
3279 Acromicric dysplasia User:Manifestation/Not checked
3280 Sialadenitis User:Manifestation/Not checked
3281 Milk allergy User:Manifestation/Not checked
3282 Hereditary pancreatitis User:Manifestation/Not checked
3283 Nail–patella syndrome User:Manifestation/Not checked
3284 Tinea manuum User:Manifestation/Not checked
3285 Folate deficiency User:Manifestation/Not checked
3286 Stargardt disease User:Manifestation/Not checked
3287 Right ventricular hypertrophy User:Manifestation/Not checked
3288 Mixed connective tissue disease User:Manifestation/Not checked
3289 AIDS-related complex User:Manifestation/Not checked
3290 Primary central nervous system lymphoma User:Manifestation/Not checked
3291 Transfusion-associated graft-versus-host disease User:Manifestation/Not checked
3292 Primitive neuroectodermal tumor User:Manifestation/Not checked
3293 Neuroendocrine tumor User:Manifestation/Not checked
3294 Fibroepithelial neoplasm User:Manifestation/Not checked
3295 Catamenial pneumothorax User:Manifestation/Not checked
3296 Extrapyramidal symptoms User:Manifestation/Not checked
3297 Combined immunodeficiencies User:Manifestation/Not checked
3298 Nezelof syndrome User:Manifestation/Not checked
3299 Shift work sleep disorder User:Manifestation/Not checked