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Genetic Disorder meaning in Urdu

Genetic Disorder Sentence

His wife has a genetic disorder.

Genetic Disorder Synonyms

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Genetic Disorder Definitions

1) Genetic Disorder, Congenital Disease, Genetic Abnormality, Genetic Defect, Genetic Disease, Hereditary Condition, Hereditary Disease, Inherited Disease, Inherited Disorder : موروثی بیماری : (noun) a disease or disorder that is inherited genetically.

Hereditary diseases list : Down syndrome, phenylketonuria, sickle-cell anemia, marfan syndrome, polycystic kidney disease, duchenne muscular dystrophy, cystic fibrosis, ankylosing spondylitis, charcot-marie-tooth disease.

Useful Words


Digestive System : وہ نظام جو خوراک کو جسم میں شامل کرتا ہے , Brain Disease : دماغی مرض , Ailment : علالت , Porphyria : پوفائرن میٹابولزم میں پیدائشی غلطی جس سے عصبی اور عضلاتی نسیج میں تبدیلیاں ہوتی ہیں , Quarantine : قرنطینہ , Allopathy : علاج بالضد , Endemic : علاقائی مرض سے متعلق , Epidemic : وبائی بیماری لوگوں کو متاثر کرنے والی , Inherit : ورثے میں پانا , Color Blindness : رنگوں میں تمیز کرنے کی قابلیت نہ ہونا , Race : جنس , Heredity : موروثی , Genetic Code : کروموسوم کے ڈی این اے کے مالیکیول میں جینیاتی مادے کا ذخیرہ ہونے کے انداز کی ترکیب کا نام ہے , Kidney Disease : گردے کا مرض , Monogenic Disease : ایک خاندانی بیماری , Kuru : مہلک دماغی بیماری , Molecular Biology : سالماتی حیاتیات , Nephroangiosclerosis : گردوں کی سوزش سے مشابہ مرض , Celiac Disease : مرض شکم , Acquired Immunity : جراثیم کے خلاف مدافعت , Allograft : انتقال عضو , Festination : رفتار میں غیر ارادی طور پر تیزی جس طرح رعشہ اور فالج کے مریضوں میں دیکھا گیا ہے , Oliguria : پیشاب کا کم اخراج , Achondroplasia : عمر کے ساتھ ہڈیاں نہ بڑھنے کی بیماری , Paralysis Agitans : رعشہ کی بیماری , Rickettsia : چھوٹے پلیومورفک جسمیے جو طفیلی ہوتے ہیں اور آرتھرو پوڈز کی گٹ کے خلیوں میں قدرتی طور پر رہتے ہیں بعض ممالیہ جانوروں اور آدمی میں امراض پیدا کرتے ہیں , Addison's Disease : ایک غدود کی بیماری , Zoonotic : وہ بیماری جو جانوروں سے انسانوں میں پھیلے , Abetalipoproteinemia : خون کی موروثی بیماری , Hepatolenticular Degeneration : خون میں تانبے کی بیماری , Albers-Schonberg Disease : مرمری ہڈیاں

Useful Words Definitions


Digestive System: the system that makes food absorbable into the body.

Digestive system related diseases : Polyps, infections, crohn disease, cancer, celiac disease, ulcerative colitis, malabsorption, diverticulitis, short bowel syndrome, peptic ulcer disease, intestinal ischemia, hiatal hernia, gastroesophageal reflux disease (GERD).

Brain Disease: any disorder or disease of the brain.

Ailment: an often persistent bodily disorder or disease; a cause for complaining.

Porphyria: a genetic abnormality of metabolism causing abdominal pains and mental confusion.

Quarantine: enforced isolation of patients suffering from a contagious disease in order to prevent the spread of disease.

Allopathy: the usual method of treating disease with remedies that produce effects differing from those produced by the disease itself.

Endemic: of or relating to a disease (or anything resembling a disease) constantly present to greater or lesser extent in a particular locality.

Epidemic: (especially of medicine) of disease or anything resembling a disease; attacking or affecting many individuals in a community or a population simultaneously.

Inherit: receive by genetic transmission.

Color Blindness: genetic inability to distinguish differences in hue.

Race: people who are believed to belong to the same genetic stock.

Heredity: the biological process whereby genetic factors are transmitted from one generation to the next.

Genetic Code: the ordering of nucleotides in DNA molecules that carries the genetic information in living cells.

Kidney Disease: a disease that affects the kidneys, in this disease the filtration function of the kidneys is affected, leading to the excessive loss of proteins, especially albumin, in the urine. This condition can result in edema (swelling) in various parts of the body, particularly in the legs, ankles, and around the eyes.

Monogenic Disease: an inherited disease controlled by a single pair of genes.

Kuru: a progressive disease of the central nervous system marked by increasing lack of coordination and advancing to paralysis and death within a year of the appearance of symptoms; thought to have been transmitted by cannibalistic consumption of diseased brain tissue since the disease virtually disappeared when cannibalism was abandoned.

Molecular Biology: the branch of biology that studies the structure and activity of macromolecules essential to life (and especially with their genetic role).

Nephroangiosclerosis: kidney disease that is usually associated with hypertension; sclerosis of the renal arterioles reduces blood flow that can lead to kidney failure and heart failure.

Celiac Disease: it is an autoimmune disorder and a chronic digestive condition that primarily affects the small intestine. It is triggered by the consumption of gluten, which is a protein found in wheat, barley, rye, and their derivatives. When individuals with celiac disease ingest gluten, their immune system responds by damaging the lining of the small intestine. This damage hinders the absorption of essential nutrients from food, leading to a range of symptoms and potential long-term health issues.

Acquired Immunity: immunity to a particular disease that is not innate but has been acquired during life; immunity can be acquired by the development of antibodies after an attack of an infectious disease or by a pregnant mother passing antibodies through the placenta to a fetus or by vaccination.

Allograft: tissue or organ transplanted from a donor of the same species but different genetic makeup; recipient`s immune system must be suppressed to prevent rejection of the graft.

Festination: involuntary shortening of stride and quickening of gait that occurs in some diseases (e.g., Parkinson's disease).

Oliguria: abnormally small production of urine; can be a symptom of kidney disease or obstruction of the urinary tract or edema or an imbalance of fluids and electrolytes in the body.

Achondroplasia: an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism.

Paralysis Agitans: a degenerative disorder of the central nervous system characterized by tremor and impaired muscular coordination.

Rickettsia: any of a group of very small rod-shaped bacteria that live in biting arthropods (as ticks and mites) and cause disease in vertebrate hosts; they cause typhus and other febrile diseases in human beings.

Addison's Disease: a glandular disorder caused by failure of function of the cortex of the adrenal gland and marked by anemia and prostration with brownish skin.

Zoonotic: zoonotic refers to diseases, infections, or agents that can be transmitted between animals and humans, posing the risk of infection or disease transmission from animals to people or vice versa.

Abetalipoproteinemia: a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels.

Hepatolenticular Degeneration: a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain.

Albers-Schonberg Disease: an inherited disorder characterized by an increase in bone density; in severe forms the bone marrow cavity may be obliterated.

Related Words


Disease : مرض

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