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Congenic Animals -- See Animals, Congenic


Animals that are produced through selective breeding to eliminate genetic background differences except for a single or few specific loci. They are used to investigate the contribution of genetic background differences to PHENOTYPE
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Congenital abnormalities -- See Abnormalities, Human



--subdivision Abnormalities under individual organs and regions of the body, e.g. Heart--Abnormalities
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Congenital Abnormalities   35
 

Congenital Abnormalities chemically induced -- See Abnormalities, Drug-Induced


Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment
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Congenital Abnormalities -- diagnosis.   4
Congenital Abnormalities -- diagnostic imaging   2
Congenital Abnormalities -- embryology   3
Congenital Abnormalities -- epidemiology : Epidemiology of human congenital malformations  2014 1
Congenital Abnormalities -- etiology   3
Congenital Abnormalities -- genetics   7
Congenital Abnormalities -- history   5
Congenital Abnormalities -- history -- Great Britain   2
Congenital Abnormalities -- mortality : The black stork : eugenics and the death of "defective" babies in American medicine and motion pictures since 1915 / Martin S. Pernick  1996 1
Congenital Abnormalities -- pathology   2
Congenital Abnormalities -- prevention & control   2
Congenital Abnormalities -- psychology : Body image and disfigurement care / Robert Newell  2000 1
Congenital Abnormalities -- rehabilitation : Studying disability : multiple theories and responses / Elizabeth DePoy, Stephen French Gilson  2011 1
Congenital Abnormalities -- surgery   2
Congenital Abnormalities -- therapy   3
 

Congenital Abnormality -- See Congenital Abnormalities


Malformations of organs or body parts during development in utero
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  Congenital Adrenal Hyperplasia -- 2 Related Subjects   2
 

Congenital Adrenal Hyperplasias -- See Adrenal Hyperplasia, Congenital


A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders
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Congenital Amauroses, Leber -- See Leber Congenital Amaurosis


A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells
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Congenital Amaurosis, Leber -- See Leber Congenital Amaurosis


A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells
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Congenital Amaurosis of Retinal Origin -- See Leber Congenital Amaurosis


A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells
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  Congenital analgesia -- 2 Related Subjects   2
 

Congenital analgia -- See Congenital insensitivity to pain


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Congenital anomalies -- See Abnormalities, Human



--subdivision Abnormalities under individual organs and regions of the body, e.g. Heart--Abnormalities
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Congenital arthromyodysplasia -- See Arthrogryposis


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Congenital Auditory Agnosia -- See Agnosia


Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities
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Congenital Auditory Agnosias -- See Agnosia


Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities
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Congenital cardiac anomalies -- See Congenital heart disease


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Congenital cardiac defects -- See Congenital heart disease


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Congenital cardiac disease -- See Congenital heart disease


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Congenital cardiac malformations -- See Congenital heart disease


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congenital Cardiovascular Diseases : Cardiovascular MRI in congenital heart disease : an imaging atlas / Shankar Sridharan [and others]  2010 1
congenital Cataract   3
 

Congenital Cerebral Palsy -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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Congenital Clubfeet -- See Clubfoot


A deformed foot in which the foot is plantarflexed, inverted, and adducted
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Congenital Clubfoot -- See Clubfoot


A deformed foot in which the foot is plantarflexed, inverted, and adducted
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congenital Colonic Neoplasms : Management of hereditary colorectal cancer : a multidisciplinary approach / Jose G. Guillem, Garrett Friedman, editors  2020 1
congenital Coronary Artery Disease : Atlas of pediatric CTA of coronary artery anomalies / Randy Ray Richardson  2020 1
congenital Cytomegalovirus Infections : Congenital cytomegalovirus infection : epidemiology, diagnosis, therapy / Gabriele Halwachs-Baumann, editor  2011 1
 

Congenital deafness -- See Deafness Genetic aspects


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Congenital Defect -- See Congenital Abnormalities


Malformations of organs or body parts during development in utero
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Congenital Defects -- See Congenital Abnormalities


Malformations of organs or body parts during development in utero
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congenital Diabetes Mellitus, Type 1 : Congenital endocrinopathies : new insights into endocrine diseases and diabetes / volume editors, Renata Lorini Genova [and others]  2007 1
congenital Dilatation, Pathologic : Pancreaticobiliary maljunction and congenital biliary dilatation / Terumi Kamisawa, Hisami Ando, editors  2018 1
 

Congenital diseases -- See Genetic disorders



--subdivision Genetic aspects under individual diseases and types of diseases, e.g. Cancer--Genetic aspects; and subdivision Diseases--Genetic aspects under organs and regions of the body, e.g. Heart--Diseases--Genetic aspects
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Congenital diseases & disorders.   2
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