Noun:

উত্তরাধিকার সুত্রে প্রাপ্ত বিশৃঙ্খলা,

inherited disorder's Usage Examples:

inherited disorder characterized by anemia with some joint and skeletal deformities.

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

This rare inherited disorder affects muscles cells.

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

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

Acromicric dysplasia is an extremely rare inherited disorder characterized by abnormally short hands and feet, growth retardation and delayed bone maturation.

Becker muscular dystrophy is an X-linked recessive inherited disorder characterized by slowly progressing muscle weakness of the legs and pelvis.

Pseudopseudohypoparathyroidism (PPHP) is an inherited disorder, named for its similarity to pseudohypoparathyroidism in presentation.

Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited disorder.

Homocystinuria or HCU is an inherited disorder of the metabolism of the amino acid methionine due to a deficiency of cystathionine beta synthase or methionine.

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

also known as 3-Methylcrotonylglycinuria or BMCC deficiency is an inherited disorder in which the body is unable to process certain proteins properly.

Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid to accumulate in the blood.

congenital cystic dilatation of the intrahepatic biliary tree) is a rare inherited disorder characterized by cystic dilatation (or ectasia) of the bile ducts.

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

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.

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

Tangier disease or hypoalphalipoproteinemia is an extremely rare inherited disorder characterized by a severe reduction in the amount of high density lipoprotein.

designed to reverse lipoprotein lipase deficiency (LPLD), a rare inherited disorder which can cause severe pancreatitis.

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

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;