Noun:

जन्मजात रोग,

congenital disease's Usage Examples:

acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.

Polysplenia is a congenital disease manifested by multiple small accessory spleens, rather than a single, full-sized.

Non-compaction cardiomyopathy (NCC), is a rare congenital disease of heart muscle that affects both children and adults.

She was born with an extremely rare congenital disease called Marfanoid–progeroid–lipodystrophy syndrome that, among other.

Although rare, the congenital disease is most prevalent among populations originating from China.

Umbilical cord ulceration and intestinal atresia is a rare congenital disease that leads to intestinal atresia, umbilical cord ulceration and severe intrauterine.

She has a vision impairment because of a congenital disease.

Dyskeratosis congenita is congenital disease characterized by reticular skin pigmentation, nail degeneration, and.

with juvenile macular dystrophy (HJMD or CDH3) is an extremely rare congenital disease characterized by sparse hair growth (hypotrichosis) from birth and.

synthesis occur in rare acquired diseases such as paroxysmal nocturnal hemoglobinuria (PNH) and congenital diseases such as hyperphosphatasia with mental.

deteriorated in 1938, after his right leg was amputated due to a congenital disease.

myopathy: is a congenital disease resulted from altered function of UDP-GlcNAc epimerase .

"bullous acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.

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, 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,