congenital

  • 81Congenital endothelial dystrophy type 1 — Classification and external resources A markedly opaque cornea due to stromal edema secondary to defective endothelial cells (Courtesy of Dr. Ahmed A. Hidajat) …

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  • 82Congenital onychodysplasia of the index fingers — is defined by the presence of the condition at birth, either unilateral or bilateral index finger involvement, variable distortion of the nail or lunula, and polyonychia, micronychia, anonychia, hemionychogryphosis, or malalignment.[1]:783 The… …

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  • 83Congenital stenosis of vena cava — Classification and external resources ICD 10 Q26.0 ICD 9 747.49 Congenital stenos …

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  • 84Congenital anomalies of spine — Classification and external resources ICD 10 Q67.5 ICD 9 756.1 Specific birth defects wh …

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  • 85Congenital fibrosis of the extraocular muscles — Congenital fibrosis of the extraocular muscles, or CFEOM, is a class of rare genetic disorders affecting one or more of the muscles that move the eyeballs. Individuals with CFEOM have varying degrees of ophthalmoplegia (an inability to move the… …

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  • 86Congenital hypoplastic anemia — Classification and external resources ICD 10 D61.0 ICD 9 284.0 …

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  • 87Congenital pulmonary airway malformation — (CPAM) is a hamartomatous lesion of the lung, with an incidence of about 1 in 5,000 live births. It can be separated into five types based on clinical and pathologic features. CPAM type 1 is the most common with large cysts and good prognosis.… …

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  • 88congenital megacolon — n HIRSCHSPRUNG S DISEASE * * * megacolon in a section of the colon due to congenital absence of intrinsic ganglion cells in the myenteric and submucosal plexuses of the next distal segment; the aganglionic part is abnormally narrow, and its loss… …

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  • 89Congenital epulis — Classification and external resources DiseasesDB 32726 The congenital epulis is a proliferation of cells on the upper jaw at birth. This is more commonly found on female babies. The cause of the disease is unknown. See also Epulis …

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  • 90Congenital estrogen deficiency — is a genetic condition by which the body is unable to produce or use estrogens.[1] Conditions include: Aromatase deficiency, a condition where the enzyme aromatase is absent and androgens are not converted to estrogens. Estrogen insensitivity… …

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