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255399007: Congenital (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Entire term case insensitive SNOMED CT core module
380599019 Congenita en Synonym Active Entire term case insensitive SNOMED CT core module
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Disorder of fatty acid metabolism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cornea globular Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of right pulmonary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hyperplasia of intrahepatic bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Infantile malignant osteopetrosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Monster with cranial anomalies Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of neck Occurrence False Congenital Inferred relationship Existential restriction modifier
Macrocolon Occurrence False Congenital Inferred relationship Existential restriction modifier
Spina bifida without hydrocephalus Occurrence False Congenital Inferred relationship Existential restriction modifier 5
Papillon-Lefèvre syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital macrostomia Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogen storage disease, type IX Occurrence False Congenital Inferred relationship Existential restriction modifier
Single vessel of umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Chronic granulomatous disease, type IA Occurrence False Congenital Inferred relationship Existential restriction modifier
Floating liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Polydactyly Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of coronary sinus Occurrence False Congenital Inferred relationship Existential restriction modifier
Gemination of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Mietens syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
4-Hydroxyphenylpyruvate dioxygenase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Annular pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Double auditory canal Occurrence False Congenital Inferred relationship Existential restriction modifier
De Lange syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
12q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of macula Occurrence False Congenital Inferred relationship Existential restriction modifier
Mongolian spot Occurrence False Congenital Inferred relationship Existential restriction modifier
Fanconi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Spondyloepiphyseal dysplasia congenita Occurrence False Congenital Inferred relationship Existential restriction modifier
Gyrate atrophy of the choroid AND/OR retina (disorder) Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of vein Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of forearm with hand AND fingers Occurrence False Congenital Inferred relationship Existential restriction modifier
Pseudocryptorchism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hepatomegaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent hyperphenylalaninemia AND tyrosinemia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Metachromatic leukodystrophy, congenital type Occurrence False Congenital Inferred relationship Existential restriction modifier
Sulfite oxidase deficiency syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of the hematopoietic system Occurrence False Congenital Inferred relationship Existential restriction modifier
Nevus anemicus Occurrence False Congenital Inferred relationship Existential restriction modifier
Primary hyperoxaluria, type II Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Argininosuccinate lyase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Omphalophlebitis Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete trisomy 21 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Holoacardius amorphus Occurrence False Congenital Inferred relationship Existential restriction modifier
Pre-eruptive color change of tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Langer-Giedion syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Dicephalus tripus tribrachius Occurrence False Congenital Inferred relationship Existential restriction modifier
Globoid cell leukodystrophy, late-onset Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Supernumerary external ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of uterus, affecting pregnancy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital esophagobronchial fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebro-oculo-facio-skeletal syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Conjoined twins Occurrence False Congenital Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Macrodactyly of toe Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomalies of fetus Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple malformation syndrome with limb defect as major feature Occurrence False Congenital Inferred relationship Existential restriction modifier
Uterus acollis Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple malformation syndrome, small stature, without skeletal dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Disseminated superficial actinic porokeratosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital supravalvular mitral stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypertrophy of sphenoid bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogen storage disease type VIII Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hyperimmunoglobulin E syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis III-A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of upper respiratory system Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of lacrimal gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Leri's pleonosteosis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome, procollagen proteinase resistant Occurrence False Congenital Inferred relationship Existential restriction modifier
Horseshoe kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
5,10-Methylenetetrahydrofolate reductase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital absence of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of endocrine gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of genital organ Occurrence False Congenital Inferred relationship Existential restriction modifier
Symbrachydactyly Occurrence False Congenital Inferred relationship Existential restriction modifier
Left ventricular-right atrial communication Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of carpal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Digital fibromatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Scaphycephaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Paraumbilical hernia with gangrene AND obstruction Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duplication of anus Occurrence False Congenital Inferred relationship Existential restriction modifier
Oligohydramnios sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
18p partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Neuronal ceroid lipofuscinosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital fusion of kidneys Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital varus deformity of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type II Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of abdominal muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Cochleate uterus Occurrence False Congenital Inferred relationship Existential restriction modifier
Eruption cyst of jaw Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duplication of cecum Occurrence False Congenital Inferred relationship Existential restriction modifier
Occipital encephalocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Methylmalonic acidemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Kartagener syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
18q partial monosomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Juvenile neurosyphilis Occurrence False Congenital Inferred relationship Existential restriction modifier
Oto-palato-digital syndrome, type II Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Cystinuria, type 3 Occurrence False Congenital Inferred relationship Existential restriction modifier
Xeroderma pigmentosum, group F Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial type 3 hyperlipoproteinemia Occurrence False Congenital Inferred relationship Existential restriction modifier

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