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Showing below up to 50 results in range #13,161 to #13,210.
- Confidence level → Confidence interval
- Confienza → Guidewire confianza
- Confluence of the sinuses → Confluence of sinuses
- Confluens sinuum → Confluence of sinuses
- Confobos → Famotidine
- Confocal Microscopy → Confocal microscopy
- Conformations → Conformation
- Conformer → Conformational isomerism
- Confounding factor → Confounding
- Confounding variable → Confounding
- Confusion laboratory tests → Confusion laboratory findings
- Confusion natural history → Confusion natural history, complications and prognosis
- Congeital Rubella Syndrome → Congenital rubella syndrome
- Congenital → Congenital disorder
- Congenital Abnormalities → Congenital disorder
- Congenital Adrenal Hyperplasia → Congenital adrenal hyperplasia
- Congenital Adrenogenital Syndrome → Congenital adrenal hyperplasia
- Congenital Amegakaryocytic Thromboytopenia (CAMT) → Thrombocytopenia
- Congenital Anomalies of the Coronary Circulation → Anomalous origins of coronary arteries
- Congenital Auricular Fistula → Preauricular sinus and cyst
- Congenital Bilateral Absence of the Vas Deferens → Congenital Absence of the Vas Deferens
- Congenital CMV infection → Congenital CMV
- Congenital Cataracts → Cataract
- Congenital Central Hypoventilaion Syndrome → Ondine's curse
- Congenital Central Hypoventilation Syndrome → Ondine's curse
- Congenital Cystic Dysplasia → Congenital cystic dysplasia
- Congenital ET → Essential thrombocytosis
- Congenital Facial Diplegia → Mobius syndrome
- Congenital Heart Disease → Congenital heart disease
- Congenital Hemiplegia → Hemiplegia
- Congenital Hyperinsulinism → Hyperinsulinism
- Congenital Lobar Emphysema → Congenital pulmonary anomalies#Congenital Lobar Emphysema
- Congenital Long QT → Long QT syndrome
- Congenital Long QT Syndrome → Long QT syndrome
- Congenital Muscular Dystrophy → Muscular dystrophy
- Congenital Myasthenic Syndrome → Congenital myasthenic syndrome
- Congenital Nephrotic Syndrome → Congenital nephrotic syndrome
- Congenital TORCH infections → TORCH complex
- Congenital Vitamin B12 Malabsorption → Vitamin B12
- Congenital abnormalities → Congenital disorder
- Congenital absence → Congenital disorder
- Congenital absence of breast with absent nipple → Amastia
- Congenital absence of skin → Aplasia cutis congenita
- Congenital adrenal hyperplasia (CAH) → Congenital adrenal hyperplasia
- Congenital adrenal hyperplasia (patient information) → Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (patient information)
- Congenital adrenal hyperplasia 1 → 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency → Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency → Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency → 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency (patient information) → 11β-hydroxylase deficiency (patient information)