| BFHD | Beukes familial hip dysplasia |
|---|---|
| DDH | developmental dysplasia of the hip; Diploma in Dental Health; dissociated double hypertropia |
| DHS | delayed hypersensitivity; diabetic hyperosmolar state; duration of hospital stay; dynamic hip screw |
| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| HIP | health illness profile; health insurance plan or program; homograft incus prosthesis; hospital insur... |
| hip pointer | Sportstalk for an iliac crest contusion (a bruise of the upper edge of the ilium, one of the hip bones). (12 Dec 1998) |
|---|---|
| hip prosthesis | Replacement for a hip joint. (12 Dec 1998) |
| hip replacement | Surgery to replace all or part of the hip joint with an artificial device that re-establishes normal hip joint motion. Indicated in cases of severe intractable degenerative arthritis (DJD). (27 Sep 1997) |
| hip tree | <botany> The dog-rose. Source: Websters Dictionary (01 Mar 1998) |
| senile hip disease | <orthopaedics> Deformity of the head of the femur caused by ischemic damage. Synonym: senile hip disease. (05 Mar 2000) |
| quiet hip disease | perthes disease |
| osteoarthritis, hip | Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterised by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. (12 Dec 1998) |
| triceps muscle of hip | <anatomy> The obturator internus and superior and inferior gemellus muscles considered as one muscle, inserting via a single tendon into the greater trochanter of the femur. Synonym: musculus triceps coxae, triceps muscle of hip. (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) |