Noun:

హెరిటేజ్ డిజార్డర్,

inherited disorder's Usage Examples:

Aase syndrome is thought to be an autosomal dominant inherited disorder.

rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT).

An example of pleiotropy is phenylketonuria, an inherited disorder that affects the level of phenylalanine, an.

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine.

as an autosomal recessively inherited disorder in a Turkish family.

Spondyloepimetaphyseal dysplasia, Strudwick type is an inherited disorder of bone growth that results in dwarfism, characteristic skeletal abnormalities.

Argininosuccinic aciduria, is an inherited disorder that causes the accumulation of argininosuccinic acid (also known as "ASA") in the blood and urine.

Crigler–Najjar syndrome is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells.

this protein have been associated with pachyonychia congenita, an inherited disorder of the epithelial tissues in which this keratin is expressed, particularly.

Congenital dysfibrinogenemia is an inherited disorder in which one of the parental genes produces an abnormal fibrinogen.

de Klerk – Gold (national reconciliation and nation-building)Basil Schonland (posthumously) – Gold (physicist and founding president of the Council for Scientific and Industrial Research)Peter Beighton – Bronze (research into the inherited disorders of the skeleton)Hamilton Naki – Bronze (medical science)2003No awards presented.

This is an inherited disorder with several different causes which define the type.

Synonyms:

branched chain ketoaciduria, achondroplasty, McArdle's disease, oligodactyly, marble bones disease, inborn error of metabolism, Fanconi's anemia, dwarfism, osteopetrosis, lactose intolerance, polygenic disorder, inherited disease, mucopolysaccharidosis, autosomal dominant disease, congenital megacolon, Albers-Schonberg disease, genetic defect, nanism, genetic abnormality, maple syrup urine disease, Hirschsprung's disease, abetalipoproteinemia, congenital afibrinogenemia, genetic disorder, achondroplasia, hepatolenticular degeneration, congenital disease, Wilson's disease, hereditary condition, Spielmeyer-Vogt disease, juvenile amaurotic idiocy, dystrophy, milk intolerance, monogenic disease, porphyria, oligodontia, hyperbetalipoproteinemia, otosclerosis, osteosclerosis congenita, polygenic disease, Fanconi's anaemia, congenital pancytopenia, autosomal recessive disease, pachyderma, hereditary disease, chondrodystrophy, autosomal recessive defect, lactase deficiency, autosomal dominant disorder, monogenic disorder, genetic disease, nevoid elephantiasis, muscular dystrophy, ichthyosis, disease,

Antonyms:

wellness,