Items without sitelinks
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Showing below up to 50 results in range #14,701 to #14,750.
- Haemolytic anaemia due to red cell diphosphoglycerate mutase deficiency (Q98109)
- Congenital displacement of the stomach due to situs inversus (Q98108)
- Unintentional water transport injury event, crushed between colliding ships (Q98107)
- Unintentional water transport injury event , hit by falling object as a result of accident to watercraft (Q98106)
- Complete absence of gastric muscle (Q98105)
- Partial absence of gastric muscle (Q98104)
- Congenital gastric atresia associated with epidermolysis bullosa (Q98103)
- Unintentional water transport injury event, struck by boat or part thereof after falling or jumping from damaged boat (Q98102)
- Mobility of bone functions (Q98101)
- Unintentional water transport injury event, burned while ship on fire (Q98100)
- Leigh syndrome with no known genetic or respiratory chain deficiency (Q98099)
- Lactate transporter deficiency (Q98098)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, unspecified watercraft (Q98097)
- Muscle endurance functions (Q98096)
- Stability of joint functions (Q98095)
- Unintentional water transport injury event, injured in watercraft accident involving collision of watercraft (Q98094)
- Unintentional water transport injury event, fall due to collision or other accident to watercraft (Q98093)
- Pulmonary autograft failure (Q98092)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, canoe or kayak (Q98091)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, water-skis (Q98090)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, other unpowered watercraft (Q98089)
- Spondylolysis with slippage with determinant, otherwise specified (Q98088)
- Idiopathic glomerular disease (Q98087)
- Spondyloptosis with slippage (Q98086)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, inflatable craft, nonpowered (Q98085)
- Iatrogenic spondylolysis with slippage (Q98084)
- Glomerular disease associated with secondary causes or systemic conditions (Q98083)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, other powered watercraft (Q98082)
- Traumatic spondylolysis with slippage (Q98081)
- Glomerular disease associated with genetic or familial disease (Q98080)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, merchant ship (Q98079)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, sailboat (Q98078)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, passenger ship (Q98077)
- Unintentional water transport injury event with water vessel damaged, disabled or destroyed, causing other injury, fishing boat (Q98076)
- Otosclerosis involving otic capsule (Q98075)
- Photoaggravated psoriasis (Q98074)
- Dilated cardiomyopathy due to lupus erythematosus (Q98073)
- Postprocedural systemic-to-pulmonary arterial shunt acquired obstruction (Q98072)
- Dilated cardiomyopathy due to juvenile rheumatoid arthritis (Q98071)
- Low basal metabolic rate (Q98070)
- Melanoma involving overlapping sites of eye or ocular adnexa (Q98069)
- Follicular psoriasis (Q98068)
- Dilated cardiomyopathy due to osteogenesis imperfecta (Q98067)
- Recurrent or persistent glomerular haematuria (Q98066)
- Bathing cramp (Q98065)
- Combined haematuria with proteinuria and albuminuria (Q98064)
- Paget disease of bone in neoplastic disease, toes (Q98063)
- Chronic proteinuria (Q98062)
- Koebner psoriasis (Q98061)
- X-linked recessive hypoparathyroidism (Q98060)
