Noun:

ಆನುವಂಶಿಕ ವೈಪರೀತ್ಯಗಳು,

genetic abnormality's Usage Examples:

solitary, and is a neoplasm resulting from a genetic mutation (or other genetic abnormality) in a single precursor cell.

The Philadelphia chromosome or Philadelphia translocation (Ph) is a specific genetic abnormality in chromosome 22 of leukemia cancer cells (particularly.

each are classified from both the altered lipid profile and by the genetic abnormality.

Two to 5% of women with POI and a premutation in FMR1, a genetic abnormality, are at risk of having a child with fragile X syndrome, the most.

- Means Latin for "freak of nature" and refers to a woman with a genetic abnormality and who is mistaken for a vampire.

A natural freak would usually have been born with a genetic abnormality, while a made freak was a person who had an artificial alteration.

Huntington"s disease, a neurodegenerative illness which is the result of a genetic abnormality, whose symptoms typically appear in mid-life.

The genetic abnormality occurs randomly in sperm or egg cells or it may occur in early embryonic.

autosomal recessive condition called Naxos disease, because this genetic abnormality can also affect the integrity of the superficial layers of the skin.

While there is no treatment to correct the genetic abnormality of this syndrome, there is the potential to treat the symptoms.

Cleidocranial dysostosis (also called cleidocranial dysplasia), a genetic abnormality in humans Central core disease, a rare neuromuscular disorder Congenital.

Philadelphia chromosome or Philadelphia translocation (Ph) is a specific genetic abnormality in chromosome 22 of leukemia cancer cells (particularly chronic myeloid.

X-chromosomes, while males only have a single X chromosome, and a genetic abnormality located on the X chromosome is much more likely to cause clinical.

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

Antonyms:

wellness,