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255399007: Congenital (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
273731000077117 congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
380598010 Congenital en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
380599019 Congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
554801000077113 congénital (valeur de l'attribut) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
congénital est un(e) (attribut) périodes de vie true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant muscular dystrophy not predominantly limb girdle survenue (attribut) True congénital Inferred relationship Some 1
X-linked limb girdle muscular dystrophy with normal dystrophin survenue (attribut) True congénital Inferred relationship Some 1
Becker muscular dystrophy (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Benign scapuloperoneal muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Congenital muscular hypertrophy-cerebral syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Ji muscular dystrophy survenue (attribut) False congénital Inferred relationship Some 1
Fukuyama congenital muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Hereditary myopathy limited to females survenue (attribut) True congénital Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Merosin deficient congenital muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Megalocornea, spherophakia, secondary glaucoma syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Agenesis of body of uterus survenue (attribut) True congénital Inferred relationship Some 1
Aplasia of body of uterus survenue (attribut) True congénital Inferred relationship Some 1
X-linked muscular dystrophy not predominantly limb girdle survenue (attribut) True congénital Inferred relationship Some 1
X-linked muscular dystrophy with limb girdle distribution survenue (attribut) True congénital Inferred relationship Some 1
Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection survenue (attribut) True congénital Inferred relationship Some 1
Benign scapuloperoneal muscular dystrophy with cardiomyopathy survenue (attribut) False congénital Inferred relationship Some 1
Hutterite type of muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
X-linked muscular dystrophy with abnormal dystrophin survenue (attribut) True congénital Inferred relationship Some 1
Scapulohumeral muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Autosomal recessive muscular dystrophy not predominantly limb girdle survenue (attribut) True congénital Inferred relationship Some 1
Congenital hereditary muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Intermediate X-linked muscular dystrophy survenue (attribut) True congénital Inferred relationship Some 1
Hereditary isolated aplastic anemia survenue (attribut) True congénital Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome survenue (attribut) True congénital Inferred relationship Some 1
McCune Albright syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Osteomesopycnosis survenue (attribut) False congénital Inferred relationship Some 3
Osteosclerosis (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Female pseudohermaphroditism survenue (attribut) True congénital Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B survenue (attribut) True congénital Inferred relationship Some 3
encéphalocèle survenue (attribut) True congénital Inferred relationship Some 1
Localized abdominal wall skin atrophy survenue (attribut) False congénital Inferred relationship Some 2
Nasal encephalocele survenue (attribut) True congénital Inferred relationship Some 1
Nasal encephalocele survenue (attribut) False congénital Inferred relationship Some 2
hydromyélocèle (trouble) survenue (attribut) False congénital Inferred relationship Some 1
Hydromyelia survenue (attribut) True congénital Inferred relationship Some 1
Congenital tracheobronchomegaly (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Congenital tracheobronchomegaly (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Microcystic renal disease (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Hydromeningomyelocele survenue (attribut) False congénital Inferred relationship Some 3
Congenital honeycomb lung (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital cystic lung survenue (attribut) True congénital Inferred relationship Some 1
Congenital spastic foot survenue (attribut) True congénital Inferred relationship Some 1
Congenital spastic foot survenue (attribut) True congénital Inferred relationship Some 2
Congenital deaf mutism survenue (attribut) True congénital Inferred relationship Some 1
Complete cleft of hard palate survenue (attribut) True congénital Inferred relationship Some 1
Bilateral incomplete cleft lip and bilateral incomplete cleft of alveolar process of maxilla (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Multiple congenital cardiac defects survenue (attribut) True congénital Inferred relationship Some 1
Incomplete bilateral cleft palate (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Congenital sensorineural hearing loss (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome survenue (attribut) True congénital Inferred relationship Some 1
Incomplete cleft palate (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Cystic testicular dysplasia survenue (attribut) True congénital Inferred relationship Some 2
Aortic orifice left side by side with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Reunion Island Larsen-like syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Reunion Island Larsen-like syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Reunion Island Larsen-like syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 2
Inferior vena cava connecting to morphological left atrium survenue (attribut) True congénital Inferred relationship Some 1
Retroesophageal pulmonary artery survenue (attribut) True congénital Inferred relationship Some 1
Aortic orifice anterior left with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Syndactyly, nystagmus syndrome due to 2q31.1 microduplication survenue (attribut) True congénital Inferred relationship Some 1
Syndactyly, nystagmus syndrome due to 2q31.1 microduplication survenue (attribut) True congénital Inferred relationship Some 2
Syndactyly, nystagmus syndrome due to 2q31.1 microduplication survenue (attribut) True congénital Inferred relationship Some 3
Stomach in central position (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Aortic orifice posterior with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Developmental displacement of brachial plexus survenue (attribut) True congénital Inferred relationship Some 1
Aortic orifice anterior right with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Aortic orifice right side by side with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Intrahepatic gallbladder survenue (attribut) True congénital Inferred relationship Some 1
Aortic orifice posterior left with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Aortic orifice anterior with respect to pulmonary orifice (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Right-sided pulmonary arterial trunk survenue (attribut) True congénital Inferred relationship Some 1
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome survenue (attribut) True congénital Inferred relationship Some 4
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome survenue (attribut) True congénital Inferred relationship Some 1
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome survenue (attribut) True congénital Inferred relationship Some 3
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome survenue (attribut) True congénital Inferred relationship Some 2
Juxtaposed atrial appendage survenue (attribut) True congénital Inferred relationship Some 1
Malalignment of aortic sinus in relation to pulmonary sinus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Combined oxidative phosphorylation defect type 11 survenue (attribut) True congénital Inferred relationship Some 1
Mixed sclerosing bone dystrophy with extra-skeletal manifestation (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Fetal spina bifida (disorder) survenue (attribut) False congénital Inferred relationship Some 2
Fetal spina bifida (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Fetal hydrocephalus (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 13 (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Hereditary hyperekplexia (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Syndactyly, polydactyly, ear lobe syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Syndactyly, polydactyly, ear lobe syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Syndactyly, polydactyly, ear lobe syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Syndactyly, polydactyly, ear lobe syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
syndrome de nævus en tache de vin, citerne cérébellomédullaire élargie, hydrocéphalie survenue (attribut) True congénital Inferred relationship Some 3
syndrome de nævus en tache de vin, citerne cérébellomédullaire élargie, hydrocéphalie survenue (attribut) True congénital Inferred relationship Some 1
syndrome de nævus en tache de vin, citerne cérébellomédullaire élargie, hydrocéphalie survenue (attribut) True congénital Inferred relationship Some 2
Paternal uniparental disomy of chromosome X survenue (attribut) True congénital Inferred relationship Some 1
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis survenue (attribut) True congénital Inferred relationship Some 1
X-linked intellectual disability due to GRIA3 mutations survenue (attribut) True congénital Inferred relationship Some 1

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