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Showing below up to 50 results in range #10,901 to #10,950.
- Congenital atresia of pulmonary vein (Q101909)
- Mucopolysaccharidoses with prominent cutaneous features (Q101908)
- Oesophageal squamous cell carcinoma in situ (Q101907)
- Acral persistent papular mucinosis (Q101906)
- Self-healing juvenile cutaneous mucinosis (Q101905)
- Lipogranuloma (Q101904)
- Invasive aspergillosis of the upper respiratory tract (Q101903)
- Squamous intraepithelial neoplasia of oesophagus, high grade (Q101902)
- Idiopathic follicular mucinosis (Q101901)
- Secondary catabolic cutaneous mucinosis (Q101900)
- Focal primary metabolic cutaneous mucinosis (Q101899)
- Invasive Aspergillus tracheobronchitis (Q101898)
- Invasive aspergillosis of the larynx (Q101897)
- Paraffinoma (Q101896)
- Invasive aspergillosis of paranasal sinuses (Q101895)
- Folinic acid-responsive seizures (Q101894)
- Aspergillus mastoiditis (Q101893)
- Congenital anomaly of inferior caval vein (Q101892)
- Mycotic corneal ulcer due to Aspergillus species (Q101891)
- Aspergillus keratitis (Q101890)
- Persistent fever (Q101889)
- African iron overload (Q101888)
- Dietary haemosiderosis (Q101887)
- Congenital anomaly of the coronary sinus (Q101886)
- Aspergillus endophthalmitis (Q101885)
- Invasive renal aspergillosis (Q101884)
- Aspergillus epidural abscess (Q101883)
- Fever with rigors (Q101882)
- Aspergillus osteomyelitis (Q101881)
- Aspergillus thyroid abscess (Q101880)
- Congenital anomaly of superior caval vein (Q101879)
- Fever with chills (Q101878)
- Aspergillus endocarditis (Q101877)
- Rupture of marginal sinus affecting fetus or newborn (Q101876)
- Ehlers-Danlos syndrome with periventricular heterotopia (Q101875)
- Mitochondrial Membrane Protein-Associated Neurodegeneration (Q101874)
- Abruptio placentae affecting fetus or newborn (Q101873)
- Ehlers-Danlos syndrome, spondylocheirodysplastic type (Q101872)
- Beta-Propeller protein-associated neurodegeneration (Q101871)
- COASY Protein-Associated Neurodegeneration (Q101870)
- Ehlers-Danlos syndrome, arthrochalasic type (Q101869)
- Ehlers-Danlos syndrome, kyphoscoliotic type (Q101868)
- Ehlers-Danlos syndrome due to tenascin-X deficiency (Q101867)
- Ehlers-Danlos syndrome, cardiac valvular type (Q101866)
- Ehlers-Danlos syndrome, classic-like type (Q101865)
- Agnogenic myeloid metaplasia (Q101864)
- Myelogenous metaplasia (Q101863)
- Pantothenate-kinase-associated neurodegeneration (Q101862)
- Ehlers-Danlos syndrome, dysfibronectinaemic type (Q101861)
- Ablatio placentae affecting fetus or newborn (Q101860)
