Items without sitelinks
From determinar.ia.br - Determine suas informações
Showing below up to 50 results in range #26,451 to #26,500.
- Nonoccupational allergic contact dermatitis due to allergenic haptens derived from plants or organic matter (Q86359)
- Dislocation of L5-S1 lumbosacral vertebrae (Q86358)
- Dislocation of L4-L5 lumbar vertebrae (Q86357)
- Dislocation of L3-L4 lumbar vertebrae (Q86356)
- Congenital pes cavus, unilateral (Q86355)
- Work and employment (Q86354)
- Juvenile enthesitis related arthritis, ANA positive (Q86353)
- Tremor due to stroke (Q86352)
- Juvenile enthesitis related arthritis, HLA B27 positive (Q86351)
- Dislocation of L1-L2 lumbar vertebrae (Q86350)
- Occupational allergic contact dermatitis due to preservatives or biocides (Q86349)
- Nodular syphilide (Q86348)
- Dislocation of L2-L3 lumbar vertebrae (Q86347)
- Gummatous syphilis (Q86346)
- Education (Q86345)
- Congenital pes cavus, bilateral (Q86344)
- Economic life (Q86343)
- Juvenile enthesitis related arthritis, HLA B27 negative (Q86342)
- Juvenile enthesitis related arthritis, ANA negative (Q86341)
- Nonoccupational allergic contact dermatitis due to preservatives or biocides (Q86340)
- Tremor due to injuries to the head (Q86339)
- Infantile stiff skin syndromes (Q86338)
- Multiple renal arteries (Q86337)
- Tremor due to multiple sclerosis (Q86336)
- Hemifield loss caused by vertebrobasilar artery (Q86335)
- Trismus (Q86334)
- Temporomandibular malocclusion (Q86333)
- Hemifield loss in migraine or epilepsy (Q86332)
- Medical facilities problem, not elsewhere classified (Q86331)
- Intermaxillary contracture (Q86330)
- Oesophageal varices with bleeding in primary biliary cholangiopathy (Q86329)
- Tremor due to Wilson’s disease (Q86328)
- Tremor due to Fragile X premutation (Q86327)
- Distal duplications of chromosome 15 (Q86326)
- Fibrous or myofibroblastic proliferations in infants or children (Q86325)
- Skin of popliteal space (Q86324)
- Health care problem, not elsewhere classified (Q86323)
- Internal carotid agenesis (Q86322)
- Primary biliary cholangitis without overlap syndrome (Q86321)
- Proximal duplications of chromosome 15 (Q86320)
- Snapping jaw (Q86319)
- Congenital anomalies of cerebral vessels, not elsewhere classified (Q86318)
- Transfer for suspected condition (Q86317)
- Lordosis with no determinant (Q86316)
- Arthralgia of temporomandibular joint (Q86315)
- Juvenile idiopathic oligoarthritis, onset persistent, ANA positive (Q86314)
- Lordosis with determinant (Q86313)
- Cerebral hyperaemia (Q86312)
- Chronic temporomandibular disorder pain (Q86311)
- Intentional self-harm by exposure to hot air or gases (Q86310)
