| CALP | congenital absence of left pericardium |
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| CAS | calcarine sulcus; calcific aortic stenosis; Cancer Attitude Survey; carbohydrate-active steroid; car... |
| CASMD | congenital atonic sclerotic muscular dystrophy |
| CAVD | complete atrioventricular dissociation; completion, arithmetic problems, vocabulary, following direc... |
| CBAVD | congenital bilateral absence of vas deferens |
| fold of chorda tympani | The fold of mucosa that surrounds the chorda tympani nerve in its course through the tympanic cavity. Synonym: plica chordae tympani. (05 Mar 2000) |
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| fold of laryngeal nerve | <anatomy, nerve> The slight fold of mucosa in the piriform recess of the pharynx that encloses the superior laryngeal nerve. Synonym: plica nervi laryngei, fold of laryngeal nerve. (05 Mar 2000) |
| fold of left vena cava | A pericardial fold lying between the left oblique vein of the atrium and the left superior pulmonary vein containing the obliterated remains of the left superior vena cava. Synonym: plica venae cavae sinistrae, Marshall's vestigial fold, vestigial fold. (05 Mar 2000) |
| fold of superior laryngeal nerve | <anatomy, nerve> The slight fold of mucosa in the piriform recess of the pharynx that encloses the superior laryngeal nerve. Synonym: plica nervi laryngei, fold of laryngeal nerve. (05 Mar 2000) |
| lateral glossoepiglottic fold | The fold of mucous membrane that extends from the margin of the epiglottis to the pharyngeal wall and base of the tongue on each side, forming the lateral boundary of the epiglottic valleculae. Synonym: plica glossoepiglottica lateralis, pharyngoepiglottic fold. (05 Mar 2000) |
| lateral nasal fold | An ectodermally covered mesenchymal swelling separating the embryonic olfactory pit from the developing eye. Synonym: lateral nasal fold, lateral nasal primordium, lateral nasal process. (05 Mar 2000) |
| lateral umbilical fold | The ridge on the peritoneal surface of the anterior abdominal wall formed by the inferior epigastric vessels. Synonym: plica umbilicalis lateralis, epigastric fold, plica epigastrica. (05 Mar 2000) |
| longitudinal fold of duodenum | A fold of mucosa on the medial wall of the descending part of the duodenum above the major duodenal papilla, probably caused by the relation to the common bile duct. Synonym: plica longitudinalis duodeni. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |