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Showing below up to 50 results in range #19,001 to #19,050.
- Drug-induced osteonecrosis, metatarsus (Q93809)
- 9724/3 (Q93808)
- Hodgkin disease, nodular sclerosis, lymphocytic depletion (Q93807)
- Classical Hodgkin lymphoma, nodular sclerosis, cellular phase (Q93806)
- Acquired arteriovenous aneurysm (Q93805)
- Injury of multiple nerves at thigh level (Q93804)
- Congenital syphilitic chorioretinitis (Q93803)
- Classical Hodgkin lymphoma, nodular sclerosis, grade 2 (Q93802)
- Myelitis due to haematobium (Q93801)
- Preaxial polydactyly of fingers (Q93800)
- Hodgkin disease, nodular sclerosis, lymphocyte predominance (Q93799)
- Congenital syphilitic choroiditis (Q93798)
- Encephalitis due to Schistosoma haematobium (Q93797)
- Injury of multiple nerves at hip level (Q93796)
- Hodgkin disease, nodular sclerosis, mixed cellularity (Q93795)
- Ruptured varicose aneurysm (Q93794)
- Malignant mesenchymal tumours of gallbladder or bile ducts (Q93793)
- Parainfectious neuroretinitis (Q93792)
- Haemolytic anaemia due to 6-phosphogluconate dehydrogenase deficiency (Q93791)
- Malignant epithelial neoplasms of aortic body or other paraganglia, unspecified type (Q93790)
- Other specified malignant neoplasms including those involving overlapping sites of biliary tract (Q93789)
- Bilharzia of ureter (Q93788)
- Schistosomiasis of bladder (Q93787)
- Malignant epithelial neoplasms of carotid body, unspecified type (Q93786)
- Atonic dyspepsia (Q93785)
- Granuloma of brain due to Schistosoma haematobium (Q93784)
- Malignant epithelial neoplasms of parathyroid gland, unspecified type (Q93783)
- Malignant epithelial neoplasms of pituitary gland, unspecified type (Q93782)
- Superior glenoid labrum lesion (Q93781)
- Vegan anaemia due to Vitamin B12 deficiency (Q93780)
- Postprandial distress syndrome (Q93779)
- Leber's idiopathic stellate neuroretinitis (Q93778)
- Strain or sprain of rotator cuff capsule (Q93777)
- Haemolytic anaemia due to glutathione reductase deficiency (Q93776)
- Strain or sprain of coracohumeral ligament (Q93775)
- Microcornea, bilateral (Q93774)
- Genetic prion disease due to prion gene mutations (Q93773)
- Osteoclastoma unknown behaviour of unspecified site (Q93772)
- Aconitase deficiency (Q93771)
- Neurocutaneous melanocytosis (Q93770)
- Alpha-ketoglutarate dehydrogenase deficiency (Q93769)
- Urological transplant procedure associated with injury or harm, open approach (Q93768)
- Bone or articular cartilage tumour, not elsewhere classified (Q93767)
- Creutzfeldt-Jakob disease encephalopathy (Q93766)
- Malignant neoplasm metastasis in stomach (Q93765)
- Fumarase deficiency (Q93764)
- Microcornea, unilateral (Q93763)
- Vibration from explosion or rupture of materials or object with undetermined intent (Q93762)
- Odontogenic tumour unknown behaviour of unspecified site (Q93761)
- High pressure jet from explosion or rupture of materials or object with undetermined intent (Q93760)
