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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
Congenital pigmentary anomaly of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa, x-linked Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of nasopharynx Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa, autosomal recessive Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital septal defect of heart Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of large intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cytomegalovirus infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Tryptophan malabsorption syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type I Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Holoacardius acormus Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent omphalomesenteric artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Subacute neuronopathic Gaucher's disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anomalous pulmonary venous drainage Occurrence False Congenital Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease, connatal variant Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperprolinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fusion of sacroiliac joint Occurrence False Congenital Inferred relationship Existential restriction modifier
Manus plana Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital syphilitic pemphigus Occurrence False Congenital Inferred relationship Existential restriction modifier
Trifid pelvis of kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
Glutamate formiminotransferase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hyperphosphatasemia tarda Occurrence False Congenital Inferred relationship Existential restriction modifier
Thoracopagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Giant kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
Short cord Occurrence False Congenital Inferred relationship Existential restriction modifier
2q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Branchial cleft cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of penis Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis III-B Occurrence True Congenital Inferred relationship Existential restriction modifier 1
10p partial monosomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Moderate steroid 21-hydroxylase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stricture of artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Common arterial trunk and separate origin of pulmonary arteries Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dislocation of one hip with subluxation of other Occurrence False Congenital Inferred relationship Existential restriction modifier
Lethal multiple pterygium syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial hypobetalipoproteinemia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Stunted embryo Occurrence False Congenital Inferred relationship Existential restriction modifier
Partial congenital absence of limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Cleft leaflet of tricuspid valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of clitoris Occurrence False Congenital Inferred relationship Existential restriction modifier
Duane's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Dermatofibrosis lenticularis disseminata Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of tongue Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Deep overbite Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital viral hepatitis B infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Megaloblastic anemia due to congenital deficiency of intrinsic factor Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Congenital anomaly of optic disc Occurrence False Congenital Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to familial storage disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Existential restriction modifier
Maternal phenylketonuria fetal effect Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of adrenal gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Ring chromosome 9 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cyst of mediastinum Occurrence False Congenital Inferred relationship Existential restriction modifier
Duplication of duodenum Occurrence False Congenital Inferred relationship Existential restriction modifier
Compound monster Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Atrial septal defect with endocardial cushion defect, partial type Occurrence False Congenital Inferred relationship Existential restriction modifier
Purine-nucleoside phosphorylase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Glycogen storage disease, hepatic form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of aortic arch Occurrence False Congenital Inferred relationship Existential restriction modifier
Hemolytic anemia with emphysema AND cutis laxa Occurrence False Congenital Inferred relationship Existential restriction modifier
Gardner syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 11 Occurrence False Congenital Inferred relationship Existential restriction modifier
Heterologous chimera Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital ptosis of upper eyelid Occurrence False Congenital Inferred relationship Existential restriction modifier
Urocanate hydratase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital esophagotracheal fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Proline dehydrogenase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectopic intestinal mucosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital vascular disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Microphthalmos Occurrence False Congenital Inferred relationship Existential restriction modifier
Tetanus omphalitis Occurrence False Congenital Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Infantile fucosidosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Atresia of foramen of Luschka Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital deformity of knee joint Occurrence False Congenital Inferred relationship Existential restriction modifier
Fragile X syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypocholesterolemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Jarcho-Levin syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Embryonic cyst of vagina Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogenosis with glucoaminophosphaturia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Occurrence False Congenital Inferred relationship Existential restriction modifier
Juvenile neuronal ceroid lipofuscinosis Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Turcot syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Exstrophy of bladder sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Muscle phosphoglycerate mutase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Rachischisis Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Ask-Upmark kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
Porphyria cutanea tarda Occurrence False Congenital Inferred relationship Existential restriction modifier
Homologous chimera Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of radius Occurrence False Congenital Inferred relationship Existential restriction modifier
Common truncus arteriosus Occurrence False Congenital Inferred relationship Existential restriction modifier
Adult neuronal ceroid lipofuscinosis Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Arterial anomaly of umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Splenogonadal fusion Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hourglass stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypoplastic left heart syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier

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