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Showing below up to 50 results in range #27,601 to #27,650.
- Salmonella enterica subspecies diarizonae (Q85209)
- Salmonelaa enterica subspecies houtenae (Q85208)
- Salmonella enterica subspecies indica (Q85207)
- Medial duplications of the long arm of chromosome 5 (Q85206)
- Rectovaginal fistula with severe scar or extensive tissue loss without anal sphincter involvement (Q85205)
- Idiopathic nodular glomerulosclerosis (Q85204)
- Rectovaginal fistula without anal sphincter involvement (Q85203)
- Proximal duplications of the long arm of chromosome 5 (Q85202)
- Rectovaginal fistula with anal sphincter involvement (Q85201)
- Salmonella enterica subspecies salamae (Q85200)
- Secondary glomerular disease with membranoproliferative glomerular changes (Q85199)
- Glomerular cholesterol embolic disease (Q85198)
- Glomerular disease with chronic global sclerosis and advanced chronic injury (Q85197)
- Benign neoplasm of pharyngeal recess (Q85196)
- Glomerular disease with appearance typical of systemic diseases classified elsewhere (Q85195)
- Ischaemic glomerular disease (Q85194)
- Benign neoplasm of nasopharyngeal roof (Q85193)
- Glomerular disease with IgA disease (Q85192)
- Glomerular disease with focal and segmental sclerosis (Q85191)
- Benign neoplasm of posterior margin of septum and choanae (Q85190)
- Glomerular disease with membranoproliferative glomerular changes (Q85189)
- Autosomal recessive congenital adrenal hypoplasia (Q85188)
- Viral keratitis (Q85187)
- Glomerular disease with minor glomerular abnormality (Q85186)
- Glomerular disease with capillary necrosis (Q85185)
- Fungal keratitis (Q85184)
- Glomerular disease with diffuse crescentic, less than 50%, glomerulonephritis (Q85183)
- Early congenital syphilis (Q85182)
- Benign neoplasm of nasopharyngeal floor (Q85181)
- Secondary keratitis or keratoconjunctivitis in other infectious diseases (Q85180)
- Benign neoplasm of adenoid (Q85179)
- Bacterial keratitis (Q85178)
- Benign neoplasm of the pharyngeal tonsil (Q85177)
- Glomerular disease with proliferative glomerular changes (Q85176)
- Glomerular disease with appearance typical of familial and genetic diseases (Q85175)
- Benign neoplasm of nasopharyngeal wall (Q85174)
- Parasitic keratitis (Q85173)
- Hypertensive emergency (Q85172)
- Hypertensive urgency (Q85171)
- X-linked congenital adrenal hypoplasia (Q85170)
- Aplasia of adrenal gland (Q85169)
- Congenital adrenocortical insufficiency (Q85168)
- Congenital absence of adrenal gland (Q85167)
- Splitting of heart sounds (Q85166)
- Precordial friction (Q85165)
- Macroscopic haematuria of unspecified origin (Q85164)
- Decreased cardiac dullness (Q85163)
- Macroscopic haematuria of urinary tract origin (Q85162)
- Azithromycin resistant Shigella (Q85161)
- Cardiac friction fremitus (Q85160)
