| CMH | cardiomyopathy, hypertrophic; community mental health [services or program]; congenital malformation... |
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| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
| inferior wall of orbit | The floor of the orbit; the shortest of the four walls of the orbit, sloping upward from the orbital margin; it is comprised of the maxilla and orbital process of the palatine bone. Synonym: paries inferior orbitae, inferior wall of orbit. (05 Mar 2000) |
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| orbit | 1. <astronomy> The path described by a heavenly body in its periodical revolution around another body; as, the orbit of Jupiter, of the earth, of the moon. 2. An orb or ball. "Roll the lucid orbit of an eye." (Young) 3. <anatomy> The cavity or socket of the skull in which the eye and its appendages are situated. 4. <zoology> The skin which surrounds the eye of a bird. Origin: L. Orbita a track or rut made by a wheel, course, circuit, fr. Orbis a circle: cf. F. Orbite. See Orb. Source: Websters Dictionary (01 Mar 1998) |
| orbit evisceration | The surgical removal of the contents of the orbit. This includes the eyeball, blood vessels, muscles, fat, nerve supply, and periosteum. It should be differentiated from eye evisceration which removes the inner contents of the eye, leaving the sclera intact. (12 Dec 1998) |
| fat body of orbit | The mass of fat contained in the orbit that contributes to the support of the eyeball. Synonym: corpus adiposum orbitae, fat body of orbit. (05 Mar 2000) |
| floor of orbit | The floor of the orbit; the shortest of the four walls of the orbit, sloping upward from the orbital margin; it is comprised of the maxilla and orbital process of the palatine bone. Synonym: paries inferior orbitae, inferior wall of orbit. (05 Mar 2000) |
| lateral wall of orbit | A triangular wall of the orbit formed by the zygomatic bone, the greater wing of the sphenoid bone, and a small part of the frontal bone; posteriorly it is bounded by the superior and inferior orbital fissures. Synonym: paries lateralis orbitae. (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) |
| rubella syndrome, congenital | Transplacental infection of the foetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalised growth retardation. (12 Dec 1998) |
| congenital | <embryology> Existing at and usually before, birth, referring to conditions that are present at birth, regardless of their causation. Origin: L. Congenitus = born together (18 Nov 1997) |