Català > malaltia genètica: 1 sentit > nom 1, state| Sentit | A disease or disorder that is inherited genetically. |
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| Específic | abetalipoproteinemia | A rare inherited disorder of fat metabolism |
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| acondroplàsia | An inherited skeletal disorder beginning before birth |
| distròfia muscular | Any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles |
| ictiosi, ictiosis | Any of several congenital diseases in which the skin is dry and scaly like a fish |
| nanisme | A genetic abnormality resulting in short stature |
| oligodoncia | congenital condition in which some of the teeth are missing |
| osteopetrosi, osteopetrosis | An inherited disorder characterized by an increase / increase / increase in bone density |
| otosclerosi, otosclerosis | hereditary disorder in which ossification of the labyrinth of the inner ear causes tinnitus and eventual deafness |
| pachyderma | thickening of the skin (usually unilateral on an extremity) caused by congenital enlargement of lymph vessel and lymph vessel obstruction |
| porfíria | A genetic abnormality of metabolism causing abdominal pains and mental confusion |
| General | afecció, malaltia, morbositat, patologia | An impairment of health or a condition of abnormal functioning |
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| Anglès | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
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| Espanyol | enfermedad genética |
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