| CCHS | congenital central hypoventilation syndrome |
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| CCVM | congenital cardiovascular malformation |
| CDA | Canadian Dental Association; Certified Dental Assistant; chenodeoxycholic acid; ciliary dyskinesia a... |
| CEP | chronic eosinophilic pneumonia; chronic erythropoietic porphyria; congenital erythropoietic porphyri... |
| CET | capital expenditure threshold; congenital eyelid tetrad |
| inferior articular surface of tibia | The quadrilateral surface on the distal end of the tibia for articulation with the talus; it is concave anteroposteriorly and broader anteriorly. Synonym: facies articularis inferior tibiae. (05 Mar 2000) |
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| intra-articular | Within the cavity of a joint. Origin: intra-+ L. Articulus, joint (05 Mar 2000) |
| intra-articular cartilage | A plate or ring of fibrocartilage attached to the joint capsule and separating the articular surfaces of the bones for a varying distance, sometimes completely; it serves to adapt two articular surfaces that are not entirely congruent. Synonym: discus articularis, articular disk, fibrocartilago interarticularis, fibroplate, interarticular fibrocartilage, intra-articular cartilage. (05 Mar 2000) |
| intra-articular fracture | Fracture occurring within a joint capsule. (05 Mar 2000) |
| intra-articular ligament of costal head | Transverse fibres extending within the capsule from the ridge between the two facets on the head of the rib to the intervertebral disk. Synonym: ligamentum capitis costae intra-articulare. (05 Mar 2000) |
| intra-articular sternocostal ligament | <anatomy> A ligament within the articular capsule between a costal cartilage and the sternum; especially well developed at second costal cartilage. Synonym: ligamentum sternocostale intra-articulare. (05 Mar 2000) |
| talar articular surface of calcaneus | Any of the three facets of the calcaneus that articulate with the overlying talus; the talar articular surface anterior and middle talar articular surface contribute to the talocalcaneonavicular joint and are separated by the tarsal sinus from the posterior talar articular surface which enters into the subtalar joint. Synonym: facies articularis talaris calcanei. (05 Mar 2000) |
| temporomandibular articular disk | The fibrocartilaginous plate that separates the joint into upper and lower cavities. Synonym: discus articularis temporomandibularis, mandibular disk, temporomandibular articular disk. (05 Mar 2000) |
| thyroidal articular surface of cricoid | One of two small circular facets on the lateral surface of the cricoid cartilage near the inferior margin of the junction of the arch and lamina for articulation with the inferior horns of the thyroid cartilage. Synonym: facies articularis thyroidea cricoideae. (05 Mar 2000) |
| juxta-articular nodules | A form of tertiary yaws that is characterised by the occurrence of nodule's on the arms and legs, situated usually near the joints. Synonym: juxta-articular nodules. (05 Mar 2000) |
| extra-articular | <anatomy> Situated outside of a joint. Source: Websters Dictionary (01 Mar 1998) |
| fibrous articular capsule | The outer fibrous part of the capsule of a synovial joint, which may in places be thickened to form capsular ligaments. Synonym: membrana fibrosa, stratum fibrosum, fibrous membrane. (05 Mar 2000) |
| fibular articular surface of tibia | The flat circular articular facet on the inferior and lateral aspect of the lateral condyle of the tibia for articulation with the head of the fibula. Synonym: facies articularis fibularis tibiae. (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) |