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Showing below up to 50 results in range #4,751 to #4,800.
- Vesicocervical fistula (Q108070)
- Spontaneous closure of ventricular septal defect (Q108069)
- Personal history of corrected congenital malformations of ear (Q108068)
- Personal history of corrected hypospadias (Q108067)
- Personal history of corrected cleft lip and palate (Q108066)
- Gonococcal bursitis, tibia (Q108065)
- Gonococcal bursitis, knee joint (Q108064)
- Gonococcal bursitis, fibula (Q108063)
- Gonococcal bursitis, elbow joint (Q108062)
- Gonococcal bursitis, humerus (Q108061)
- Gonococcal bursitis, metacarpus (Q108060)
- Gonococcal bursitis, fingers (Q108059)
- Gonococcal bursitis, carpus (Q108058)
- Gonococcal bursitis, hip joint (Q108057)
- Gonococcal bursitis, sacroiliac joint (Q108056)
- Gonococcal bursitis, pelvis (Q108055)
- Gonococcal bursitis, buttock (Q108054)
- Gonococcal bursitis, femur (Q108053)
- Gonococcal bursitis, sternoclavicular joint (Q108052)
- Gonococcal bursitis, glenohumeral joint (Q108051)
- Gonococcal bursitis, acromioclavicular joint (Q108050)
- Gonococcal bursitis, ulna (Q108049)
- Gonococcal bursitis, radius (Q108048)
- Gonococcal bursitis, clavicle (Q108047)
- Gonococcal bursitis, scapula (Q108046)
- Gonococcal bursitis, wrist joint (Q108045)
- Gonococcal bursitis, other joints in foot (Q108044)
- Gonococcal bursitis, toes (Q108043)
- Gonococcal bursitis, ankle joint (Q108042)
- Gonococcal bursitis, metatarsus (Q108041)
- Gonococcal bursitis, tarsus (Q108040)
- Neuroendocrine tumour, G2 of oesophagus (Q108039)
- Neuroendocrine tumour, G1 (carcinoid) of oesophagus (Q108038)
- Small cell neuroendocrine carcinoma of oesophagus (Q108037)
- Large cell neuroendocrine carcinoma of oesophagus (Q108036)
- Acquired Von Willebrand disease due to stenotic aortic valve or cardiac malformation (Q108035)
- 9341/1 (Q108034)
- Acquired Von Willebrand disease due to myeloproliferative neoplasm or reactive thrombocytosis (Q108033)
- Epidural abscess due to tuberculosis (Q108032)
- Subacute coronary insufficiency (Q108031)
- Danish type familial amyloid cardiomyopathy (Q108030)
- Myasthenic syndromes in diabetic amyotrophy (Q108029)
- Myasthenic syndromes in hyperthyroidism (Q108028)
- Familial hypophosphatemic bone disease (Q108027)
- Hyperphosphatemia (Q108026)
- Renal hypophosphatemia (Q108025)
- Hypophosphatemia, not otherwise specified (Q108024)
- Noncompaction cardiomyopathy due to Barth syndrome (Q108023)
- Osteonecrosis in Caisson disease of the knee joint (Q108022)
- Osteonecrosis in Caisson disease of the tibia (Q108021)
