Noun:

ਜੈਨੇਟਿਕ ਵਿਕਾਰ,

genetic disorder's Usage Examples:

Myotonic dystrophy is a type of muscular dystrophy, a group of long-term genetic disorders that impair muscle function.

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited genetic disorder that predisposes those affected to potentially life-threatening.

genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and.

the inherited genetic disorders that can cause colorectal cancer include familial adenomatous polyposis and hereditary non-polyposis colon cancer; however.

Various types of hemophilia and von Willebrand disease are the major genetic disorders associated.

mucopolysaccharidosis Type IH (MPS-IH), Hurler"s disease, and formerly gargoylism, is a genetic disorder that results in the buildup of large sugar molecules.

Nail–patella syndrome is a genetic disorder that results in small, poorly developed nails and kneecaps, but can also affect many other areas of the body.

Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype.

familial dyslipidemia) is a genetic disorder characterized by the liver overproducing very-low-density lipoproteins (VLDL).

Asthma is a complex genetic disorder that has been associated with IL-4 gene promoter polymorphism and proteins involved in IL-4 signaling.

Wilson"s disease is a genetic disorder in which excess copper builds up in the body.

autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube.

resulting in a genetic disorder known as adenosine deaminase severe combined immunodeficiency disease (ADA-SCID).

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, 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, inherited disorder, genetic disease, nevoid elephantiasis, muscular dystrophy, ichthyosis, disease,

Antonyms:

wellness,