A disease or disorder that is inherited genetically, congenital disease; genetic abnormality; genetic defect; genetic disease; genetic disorder; hereditary condition; hereditary disease; inherited disease; inherited disorder. Hyponyms (each of the following is a kind of "hereditary disease"): oligodontia (congenital condition in which some of the teeth are missing), hepatolenticular degeneration; Wilson's disease (a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain), porphyria (a genetic abnormality of metabolism causing abdominal pains and mental confusion), lactase deficiency; lactose intolerance; milk intolerance (congenital disorder consisting of an inability to digest milk and milk products; absence or deficiency of lactase results in an inability to hydrolyze lactose), dwarfism; nanism (a genetic abnormality resulting in short stature), nevoid elephantiasis; pachyderma (thickening of the skin (usually unilateral on an extremity) caused by congenital enlargement of lymph vessel and lymph vessel obstruction), Albers-Schonberg disease; marble bones disease; osteopetrosis (an inherited disorder characterized by an increase in bone density; in severe forms the bone marrow cavity may be obliterated), congenital afibrinogenemia (a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma), juvenile amaurotic idiocy; Spielmeyer-Vogt disease (a congenital progressive disorder of lipid metabolism having an onset at age 5 and characterized by blindness and dementia and early death), congenital pancytopenia; Fanconi's anaemia; Fanconi's anemia (a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow), autosomal recessive defect; autosomal recessive disease (a disease caused by the presence of two recessive mutant genes on an autosome), autosomal dominant disease; autosomal dominant disorder (a disease caused by a dominant mutant gene on an autosome), otosclerosis (hereditary disorder in which ossification of the labyrinth of the inner ear causes tinnitus and eventual deafness), monogenic disease; monogenic disorder (an inherited disease controlled by a single pair of genes), oligodactyly (congenital condition in which some fingers or toes are missing), dystrophy; muscular dystrophy (any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles), McArdle's disease (an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle; results in weakness and cramping), branched chain ketoaciduria; maple syrup urine disease (an inherited disorder of metabolism in which the urine has a odor characteristic of maple syrup; if untreated it can lead to mental retardation and death in early childhood), ichthyosis (any of several congenital diseases in which the skin is dry and scaly like a fish), hyperbetalipoproteinemia (a genetic disorder characterized by high levels of beta-lipoproteins and cholesterol; can lead to atherosclerosis at an early age), mucopolysaccharidosis (any of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysaccharides in tissues), congenital megacolon; Hirschsprung's disease (congenital condition in which the colon does not have the normal network of nerves; there is little urge to defecate so the feces accumulate and cause megacolon), inborn error of metabolism (any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism), abetalipoproteinemia (a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels), achondroplasia; achondroplasty; chondrodystrophy; osteosclerosis congenita (an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism), polygenic disease; polygenic disorder (an inherited disease controlled by several genes at once).

Basic therapy for hereditary diseases includes the elimination or restriction of the intake of substances whose chemical transformation in the body, in the absence of an essential enzyme, results in a pathological condition; replacement therapy for a deficient enzyme or normal end product of a distorted reaction; and induction of deficient enzymes. I want him to help to enjoy his life.

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A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Rare hereditary disease characterized by extreme sensitivity to ionizing radiation or radiomimetic drugs because of a defect in DNA repair. Thus, not all the types of human hereditary diseases fit into the schemata listed above. The nosologie classification of hereditary diseases is the result of comprehensive clinical (including clinical-genealogical) and laboratory examinations.
  The noun HEREDITARY DISEASE has 1 sense: 1. a disease or disorder that is inherited genetically.

My mother was diagnosed with FMS and I would like to know what are the chances I’ll have it too.

Of great importance in diagnosis are biochemical, electrophysiological, cytomorphological, immunological, and other laboratory methods that frequently make it possible to identify not only the disease but the heterozygous carrier state of the mutant gene. Get unrestricted access to all the English-Learning Units! Great hopes rest on the future application of genetic engineering, that is, the planned intervention in the structure and function of the genetic apparatus, which entails the elimination or correction of mutant genes and their replacement with normal ones.

Pathological heredity can be traced vertically in the genealogy. Is FMS heredetery? Hereditary diseases are caused primarily by chromosomal and gene mutations; a distinction is made, accordingly, between chromosomal and strictly hereditary (gene) diseases. All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. Hereditary diseases are disorders or diseases that are inherited genetically. 3.5 to 4.7:1000 live births have blood hereditary diseases and 60% of the Sultanate's population have genes for genetic blood disorders.The most common genetic blood disorder in the Omani society is the G6PD deficiency as 28% of males and 12% of females have the gene of the disease. Hereditary diseases are caused primarily by chromosomal and gene mutations; a distinction is made, accordingly, between chromosomal and strictly hereditary (gene) diseases. Diseases of this type occur with equal frequency among boys and girls. However, the biochemical mechanisms of most hereditary diseases are still unknown; consequently, a pathogenetic classification cannot as yet be complete. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional. The following principal types of inheritance are distinguished according to the location of the pathological (mutant) gene—in an autosomal or in a sex chromosome—and according to its relations with the normal allele, that is, whether the mutation is dominant (the normal gene is suppressed by a pathological gene) or recessive (the pathological gene is suppressed by a normal gene): autosomal-dominant, autosomal-recessive, and sex-linked (or limited to sex). Dictionary entry overview: What does hereditary disease mean? This phenomenon is called pseudodominance. diseases caused by disturbances in the storage, transmission, and production of genetic information.

The aforementioned types of inheritance apply mainly to monogenic diseases (determined by the mutation of a single gene).