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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 group A hemolytic streptococcal pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital group B hemolytic streptococcal pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital Escherichia coli pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital chlamydial pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cardiac failure Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypertonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Perimembranous ventricular septal defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Single muscular ventricular septum defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple muscular ventricular septum defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Altered passive eruption of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, hypocalcification type Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, hypomaturation type Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, hypoplastic type Occurrence False Congenital Inferred relationship Existential restriction modifier
Generalized failure of tooth eruption associated with systemic disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Buccal bifurcation cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Riedel's lobe of liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired myelocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital auditory imperception Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital myasthenic syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital end-plate acetylcholine receptor deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital end-plate acetylcholinesterase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital and developmental anomalies of the nervous system Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dysarthria Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lattice corneal dystrophy, isolated form Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stationary night blindness Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypertrophy of retinal pigment epithelium Occurrence False Congenital Inferred relationship Existential restriction modifier
Infantile esotropia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Esotropia with dissociated vertical deviation Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Esotropia with nystagmus Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Esotropia with nystagmus block Occurrence False Congenital Inferred relationship Existential restriction modifier 2
General fibrosis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Strabismus fixus Occurrence False Congenital Inferred relationship Existential restriction modifier
Vertical retraction syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital axial myopia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital color blindness Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital vocal cord palsy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital chylothorax Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital His bundle tachycardia Occurrence False Congenital Inferred relationship Existential restriction modifier
Lymphatic malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
True congenital varicose veins Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Congenital factor IX deficiency variant Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital factor IX deficiency with inhibitor Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital von Willebrand's disease Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital von Willebrand's disease type I Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital von Willebrand's disease type II Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital von Willebrand's disease type III Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital fibrinogen abnormality Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypofibrinogenemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Alpha chain defect dysfibrinogenemia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Beta chain defect dysfibrinogenemia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Gamma chain defect dysfibrinogenemia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Leukocyte adhesion deficiency - type 1 Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Leukocyte adhesion deficiency - type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - recessive - rough Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypomaturation - recessive pigmented Occurrence False Congenital Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypomaturation - snow capped teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital microvillous atrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial absence of villi Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIB Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIC Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIIA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIIB Occurrence False Congenital Inferred relationship Existential restriction modifier
Pericellular fibrosis of congenital syphilis Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Congenital disorder of gallbladder and biliary tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Polycystic disease of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malformation of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Cystic fibrosis of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Pulmonic stenosis and congenital nephrosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital male infertility Occurrence False Congenital Inferred relationship Existential restriction modifier
Male infertility of chromosomal origin Occurrence False Congenital Inferred relationship Existential restriction modifier
Male infertility of genetic origin Occurrence False Congenital Inferred relationship Existential restriction modifier
Azoospermia with absent vasa in association with cystic fibrosis trait Occurrence False Congenital Inferred relationship Existential restriction modifier
Male infertility of developmental origin Occurrence False Congenital Inferred relationship Existential restriction modifier
Rudimentary testes associated with infertility Occurrence False Congenital Inferred relationship Existential restriction modifier
Androgen resistance - infertile male Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Primary spermatogenic failure Occurrence False Congenital Inferred relationship Existential restriction modifier
Oligosynaptic infertility Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital impairment of sperm motility Occurrence False Congenital Inferred relationship Existential restriction modifier
Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital obstructive azoospermia Occurrence False Congenital Inferred relationship Existential restriction modifier
Morbidly adherent placenta Occurrence False Congenital Inferred relationship Existential restriction modifier
Placenta adherent to previous uterine scar Occurrence False Congenital Inferred relationship Existential restriction modifier
Feminization-adrenogenital syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Virilization-adrenogenital syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital adrenal hyperplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Salt-losing congenital adrenal hyperplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Late onset congenital adrenal hyperplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital adrenal hyperplasia - desmolase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic parathyroid hormone-related protein secretion Occurrence False Congenital Inferred relationship Existential restriction modifier
Growth hormone receptor absent Occurrence False Congenital Inferred relationship Existential restriction modifier
Growth hormone receptor abnormality Occurrence False Congenital Inferred relationship Existential restriction modifier
Pterygium of nail Occurrence False Congenital Inferred relationship Existential restriction modifier

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