KMLE Medical Dictionary

 
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Abbreviations
        Did you mean: congenitally

KMLE Web Definition Match-Search Results : 5       Page: 1

congenital:
present at birth but not necessarily hereditary; acquired during fetal development
Link: wordnet.princeton.edu/perl/webwn
congenital afibrinogenemia:
a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma
Link: wordnet.princeton.edu/perl/webwn
congenital anomaly:
birth defect: a defect that is present at birth
Link: wordnet.princeton.edu/perl/webwn
congenital defect:
birth defect: a defect that is present at birth
Link: wordnet.princeton.edu/perl/webwn
congenital disease:
genetic disease: a disease or disorder that is inherited genetically
Link: wordnet.princeton.edu/perl/webwn
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KMLE Web Definition Similar-Search Results : 5       Page: 1

ringform congenital cataract:
a very rare opacity in which the lens nucleus is absent, and only a doughnut-shaped remnant of lens is left.
Link: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
Fukuyama type congenital muscular dystrophy:
an autosomal recessive type of muscular dystrophy evident in infancy; muscle abnormalities resemble those of Duchenne's muscular dystrophy, and patients are mentally retarded with polymicrogyria and other cerebral abnormalities. Called also Fukuyama's syndrome.
Link: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
adrenal hyperplasia, congenital:
A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form.(12 Dec 1998)
Link: cancerweb.ncl.ac.uk/omd/
alopecia congenitalis:
Absence of all hair at birth, associated with psychomotor epilepsy; autosomal dominant inheritance.Synonym: congenital baldness, hypotrichiasis.(05 Mar 2000)
Link: cancerweb.ncl.ac.uk/omd/
alopecia triangularis congenitalis:
A congenital triangular patch of baldness on the frontal or temporal region of the scalp.(05 Mar 2000)
Link: cancerweb.ncl.ac.uk/omd/
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MeSH(Medical Subject Headings) Match-Search (http://www.nlm.nih.gov) Results: 2       Page: 1
Congenital Hypothyroidism:
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
Synonyms: Endemic Cretinism, Cretinism, Endemic, Hypothyroidism, Congenital
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities:
Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed ABNORMALITIES.
Synonyms: Disorders, Congenital, Congenital Disorder, Disorder, Congenital
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MeSH(Medical Subject Headings) Similar-Search (http://www.nlm.nih.gov) Results: 5       Page: 1
Abnormalities:
Congenital malformations of organs or parts.
Synonyms: Abnormalities, Congenital,Congenital Abnormalities,Defects, Congenital,Abnormality,Abnormality, Congenital,Birth Defect,Congenital Abnormality,Congenital Defect,Defect, Birth,Defect, Congenital,Defects, Birth,Deformity

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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. The most common defect is in STEROID 21-HYDROXYLASE. Other defects occur in STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; or 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES).
Synonyms: Congenital Adrenal Hyperplasia,Hyperplasia, Congenital Adrenal,Adrenal Hyperplasias, Congenital,Congenital Adrenal Hyperplasias,Hyperplasias, Congenital Adrenal

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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.
Synonyms: Agnosia for Pain,Agnosia for Smell,Agnosia for Taste,Agnosia for Temperature,Auditory Agnosia, Congenital,Body-Image Agnosia,Congenital Auditory Agnosia,Developmental Agnosia,Ideational Agnosia,Olfactory Agnosia,Position Agnosia,Somatosensory Agnosia

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Amino Acid Metabolism, Inborn Errors:
Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life.
Synonyms: Amino Acid Metabolism Disorders, Inborn,Amino Acid Metabolism, Inborn Error,Amino Acid Metabolism, Inherited Disorders,Amino Acidopathies, Inborn,Congenital Amino Acidopathies,Inborn Errors, Amino Acid Metabolism,Amino Acidopathy, Congenital

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Anemia, Dyserythropoietic, Congenital:
A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PROGENITOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
Synonyms: Anemia, Congenital Dyserythropoietic,Anemia, Congenital Dyserythropoietic, Type II,Anemia, Dyserythropoietic, Congenital, Type I,Anemia, Dyserythropoietic, Congenital, Type II,Anemia, Dyserythropoietic, Congenital, Type III

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External LinkOut - Stedman's Medical Dictionary Match-Search (http://www.stedmans.com) Results: 5       Page: 1
congenital:

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congenital adrenal hyperplasia:

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congenital afibrinogenemia:

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congenital amputation:

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congenital anemia:

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bullous congenital ichthyosiform erythroderma:

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double congenital athetosis:

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nyctalopia with congenital myopia:

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poikiloderma congenitale:

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alopecia congenitalis:

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External LinkOut - CancerWeb Medical Dictionary Match-Search (http://cancerweb.ncl.ac.uk/omd/) Results: 5       Page: 1
congenital:

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congenital absence of pulmonary valve:

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congenital adrenal hyperplasia:

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congenital afibrinogenaemia:

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congenital amputation:

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External LinkOut - CancerWeb Medical Dictionary Similar-Search (http://cancerweb.ncl.ac.uk/omd/) Results: 5       Page: 1
adrenal hyperplasia, congenital:

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anaemia, dyserythropoietic, congenital:

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anaemia, haemolytic, congenital:

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anaemia, haemolytic, congenital nonspherocytic:

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bovine congenital ataxia:

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External LinkOut - Merriam-Webster's Medical Dictionary Match-Search (http://www.nlm.nih.gov/medlineplus) Results: 4       Page: 1
congenital:

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congenital contractural arachnodactyly:

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congenital megacolon:

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congenitally:

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External LinkOut - MedicineNet.com Medical Dictionary Match-Search (http://www.medicinenet.com) Results: 5       Page: 1
Congenital:

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Congenital achromatopsia,:

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Congenital anemia:

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Congenital anemia and triphalangeal thumbs:

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Congenital anemia with spinocerebellar ataxia:

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External LinkOut - MedicineNet.com Medical Dictionary Similar-Search (http://www.medicinenet.com) Results: 5       Page: 1
Anemia, congenital:

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Anomaly, congenital:

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Deafness, congenital:

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Disease, congenital heart:

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Dislocation, congenital hip:

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External LinkOut - A.D.A.M. Medical Encyclopedia Match-Search (http://www.nlm.nih.gov) Results: 20       Page: 1
Congenital adrenal hyperplasia:

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Congenital afibrinogenemia:

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Congenital antithrombin III deficiency:

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Congenital bronchiectasis:

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Congenital cataract:

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Congenital CMV:

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Congenital cranial osteoporosis:

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Congenital cytomegalovirus:

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Congenital dermal melanocytosis:

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Congenital dislocation of the hip:

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Congenital dysplasia of the hip:

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Congenital erythropoietic porphyria:

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Congenital giant pigmented nevus:

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Congenital glaucoma:

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Congenital heart defect corrective surgery:

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Congenital heart disease:

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Congenital hernia of the diaphragm:

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Congenital herpes:

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Congenital hypertrophic pyloric stenosis:

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Congenital hypothyroidism:

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External LinkOut - A.D.A.M. Medical Encyclopedia Similar-Search (http://www.nlm.nih.gov) Results: 9       Page: 1
Antithrombin III deficiency - congenital:

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Cataract - congenital:

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CMV - congenital:

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Deficiency - antithrombin III - congenital:

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Diaphragmatic hernia repair - congenital:

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Herpes - congenital:

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Nephrogenic diabetes insipidus - congenital:

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Nephrotic syndrome - congenital:

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Platelet function defects - congenital:

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External LinkOut - MedlinePlus Health Topics Match-Search (http://www.nlm.nih.gov) Results: 2       Page: 1
Congenital Adrenal Hyperplasia:

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Congenital Heart Defects:

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Heart Diseases, Congenital:

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KMLE Abbreviations Similar-Search Results: 5       Page: 1
ACED:

 
anhydrotic congenital ectodermal dysplasia
 

CAH:

 
  1) Chronic Active Hepatitis
  2) Congenital Adrenal Hyperplasia
 

CALP:

 
congenital absence of left pericardium
 

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KMLE Automated Recognition Abbreviations Similar-Search Results: 5       Page: 1
C.C.A.M.:

 
Congenital Cystic Adenomatoid Malformation
 

C.M.:

 
Congenital Malformations
 

CAVD:

 
Congenital absence of the vas deferens
 

CBAVD:

 
Congenital bilateal absence of the vas deferens
 

CCA:

 
Congenital contractural arachnodactyly
 

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Journal Abbreviations(Pubmed/Entrez) Search Results: 1       Page: 1

JrId: 29811
JournalTitle: Congenital anomalies.
MedAbbr: Congenit Anom (Kyoto)
ISSN: 0914-3505
ESSN:
IsoAbbr:
NlmId: 9306292

         
WHO ICD-10 Version 2006 Match-Search (http://www.who.int) Results: 5       Page: 1
A50.-: Congenital syphilis
A50.9: Congenital syphilis, unspecified
D64.4: Congenital dyserythropoietic anemia
D74.0: Congenital methemoglobinemia
E00.-: Congenital iodine-deficiency syndrome
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WHO ICD-10 Version 2006 Similar-Search (http://www.who.int) Results: 5       Page: 1
A50.0: Early congenital syphilis, symptomatic
A50.1: Early congenital syphilis, latent
A50.2: Early congenital syphilis, unspecified
A50.3: Late congenital syphilitic oculopathy
A50.4: Late congenital neurosyphilis [juvenile neurosyphilis]
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WordNet English Dictionary Similar-Search Results: 10       Page: 1
congenital: present at birth but not necessarily hereditary
congenital: a defect that is present at birth
congenital: a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma
congenital: a defect that is present at birth
congenital: a defect that is present at birth
congenital: a disease or disorder that is inherited genetically
congenital: a defect that is present at birth
congenital: a birth defect involving the heart
congenital: congenital condition in which the colon does not have the normal network of nerves
congenital: a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow
         
External LinkOut - American Heritage Dictionary Match-Search (http://www.yahoo.com) Results: 4       Page: 1
congenital:

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congenital anomaly:

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congenital myxedema:

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congenitally:

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