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From determinar.ia.br - Determine suas informações
Showing below up to 50 results in range #15,851 to #15,900.
- DEND - [Developmental delay - epilepsy - neonatal diabetes] syndrome (Q96959)
- Lyme arthritis, radius (Q96958)
- Lyme arthritis, clavicle (Q96957)
- Lyme arthritis, glenohumeral joints (Q96956)
- Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Q96955)
- Lyme arthritis, sternoclavicular joints (Q96954)
- Unspecified malignant tumour of soft tissue or sarcoma of posterior mediastinum (Q96953)
- Lyme arthritis, ulna (Q96952)
- Lyme arthritis, elbow joint (Q96951)
- Sigmoid hypertrophy (Q96950)
- Unspecified malignant soft tissue or sarcoma involving overlapping sites of heart, mediastinum or non-mesothelioma of pleura (Q96949)
- Unspecified malignant tumour of soft tissue or sarcoma of heart (Q96948)
- Rectal dilatation (Q96947)
- Cecum dilatation (Q96946)
- Lyme arthritis, humerus (Q96945)
- Lyme arthritis, wrist joint (Q96944)
- Unspecified malignant soft tissue or sarcoma of pleura (Q96943)
- Lyme arthritis, acromioclavicular joints (Q96942)
- Ileal Arteries (Q96941)
- Jejunal arteries (Q96940)
- Colonic dilatation (Q96939)
- Drug-induced or toxic liver disease with acute fatty liver disease, without complications (Q96938)
- Vaginitis due to Trichomonas vaginalis (Q96937)
- Trichomonal vulvovaginitis (Q96936)
- Trichomonal vulvitis (Q96935)
- Pineal gland dysfunction (Q96934)
- Trichomonal dysentery (Q96933)
- Trichomonal cervicitis (Q96932)
- Hypopinealism (Q96931)
- Atypical pyoderma gangrenosum of the hands (Q96930)
- Pineal syndrome (Q96929)
- Cystitis in trichomoniasis (Q96928)
- Urethritis due to Trichomonas vaginalis (Q96927)
- Onychotillomania (Q96926)
- Carbonic anhydrase II deficiency (Q96925)
- Drug-induced or toxic liver disease with acute fatty liver disease, with complications (Q96924)
- Genital trichomoniasis female (Q96923)
- Trichomonal colitis (Q96922)
- Pineal gland calcification (Q96921)
- Familial camptodactyly (Q96920)
- Proximal renal tubular acidosis due to familial or genetic disease (Q96919)
- Hyperpinealism (Q96918)
- Voluntary or psychogenic flutter (Q96917)
- Sporadic camptodactyly (Q96916)
- Macrocornea with glaucoma (Q96915)
- Macrophthalmos in congenital glaucoma (Q96914)
- Pineal gland degeneration (Q96913)
- Epiphysis cerebri cyst (Q96912)
- Congenital glaucoma associated with homocystinuria (Q96911)
- Streblodactyly (Q96910)
