familial disease

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Related to familial disease: Autosomal disease

familial disease

A disease that occurs in several members of the same family.


occurring in or affecting members of a closely related group of animals more than would be expected by chance.

familial aggregations
groups of diseased animals concentrated in related groups of animals. Called also familial clusters.
Basenji familial anemia
see familial nonspherocytic anemia of Basenji dogs.
familial cluster
see familial aggregations (above).
familial convulsions and ataxia of cattle
an inherited, congenital disease of Aberdeen Angus calves characterized by intermittent tetanic convulsions which are replaced as the calf gets older by incoordination and then paralysis in older animals. The characteristic lesion is a selective cerebellar cortical degeneration.
familial disease
diseases which occur at a higher than expected frequency in closely related groups of animals, where the relationship is a shared environment or an inheritance.
familial glomerulonephritis
of Dobermans characterized by development of signs in dogs less than a year old but cases may survive for some years; the histopathological lesion is a membranoproliferative glomerulonephritis.
familial renal disease
includes familial glomerulonephritis, nephropathy, juvenile nephropathy, all of dogs, familial glomerulonephritis of Finnish-Landrace sheep, progressive renal fibrosis of mutant Southdown sheep.
References in periodicals archive ?
Arrhythmogenic right ventricular cardiomyopathy is a familial disease characterized by dilatation and regional wall hypokinesia of the right ventricle and left bundle branch block VT on ECG.
The FISH technique potentially extends the usefulness of PGD far beyond couples with a known familial disease to those concerned about miscarriage or birth defects associated with advanced maternal age or a history of recurrent pregnancy loss.
Families of people who succumb to sudden arrhythmic death syndrome should be assessed for cardiac disease, because one in five such families could be found to have occult familial disease, reported Dr.
Testing for the presence of familial disease variants can determine risk in young family members and help prevent sudden cardiac death through timely intervention.
Amyloidosis cutis dyschromica is assumed to be a familial disease with sunlight exposure as a major etiological factor.

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