Noun:

জন্মগত বিশৃঙ্খলা,

congenital disorder's Usage Examples:

A congenital disorder of glycosylation (previously called carbohydrate-deficient glycoprotein syndrome) is one of several rare inborn errors of metabolism.

Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation.

Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig) characterized by abnormal N-glycosylation.

Microcheilia is a congenital disorder where one's lips are unusually small.

mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency".

Clinically, the deficiency of ALG1 in humans results in ALG1-CDG, a congenital disorder of glycosylation.

A birth defect, also known as a congenital disorder, is a condition present at birth regardless of its cause.

Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih).

anemia is a type of aplastic anemia which is primarily due to a congenital disorder.

-ia) is a congenital disorder of a limb resulting from a disturbance in embryonic development.

"Subcutaneous fat pads on body MRI--an early sign of congenital disorder of glycosylation PMM2-CDG (CDG1a)".

Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair growth and dental development.

cyclopes) is the most extreme form of holoprosencephaly and is a congenital disorder (birth defect) characterized by the failure of the embryonic prosencephalon.

called osteosclerotic bone dysplasia, is a rare autosomal recessive congenital disorder characterized by craniofacial anomalies including microcephaly, noticeably.

A congenital lip pit or lip sinus is a congenital disorder characterized by the presence of pits and possibly associated fistulas in the lips.

Zimmermann–Laband syndrome (ZLS), is an extremely rare autosomal dominant congenital disorder.

syndrome or albinism and deafness of Tietz, is an autosomal dominant congenital disorder characterized by deafness and leucism.

Nevus anemicus is a congenital disorder characterized by macules of varying size and shape that are paler than the surrounding skin and cannot be made.

A persistent cloaca is a symptom of a complex anorectal congenital disorder, in which the rectum, vagina, and urinary tract meet and fuse, creating a.

Synonyms:

congenital abnormality; anomaly; hermaphroditism; cleft lip; colour blindness; epispadias; Down syndrome; encephalocele; spina bifida; syndactyly; clinocephaly; spinocerebellar disorder; anencephalia; syndactylism; ametria; hyperdactyly; schistorrhachis; scaphocephaly; rachischisis; congenital defect; birth defect; anomalousness; Down's syndrome; ablepharia; meningocele; plagiocephaly; colour vision deficiency; mongolism; cheiloschisis; clinodactyly; amelia; cleft palate; anencephaly; meromelia; trisomy 21; macroglossia; congenital anomaly; clinocephalism; color vision deficiency; oxycephaly; hermaphrodism; tongue tie; color blindness; polysomy; congenital heart defect; myelomeningocele; polydactyly; acrocephaly; albinism; mongolianism; harelip; pseudohermaphroditism; ankyloglossia; defect;

Antonyms:

normality; hyperpigmentation; perfection; advantage;