FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.6  |  FHIR Version n/a  User: [n/a]

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
Umbilical polyp of newborn Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital uremia Occurrence False Congenital Inferred relationship Existential restriction modifier
Idiopathic hyperphosphatasemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital deformity Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetal postural deformity Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital viral disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital human parvovirus infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital coxsackie infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital acquired immune deficiency syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital human immunodeficiency virus positive status syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital non-A non-B hepatitis infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Bacterial sepsis of newborn Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital non-bacterial non-viral infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital falciparum malaria Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital candidiasis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital syphilitic rhinitis Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetal cytomegalovirus syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysmorphism Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebral dysgenesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Intrahepatic biliary hypoplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Embryological remnant Occurrence False Congenital Inferred relationship Existential restriction modifier
Ruptured cerebral arteriovenous malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Ruptured spinal arteriovenous malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysmorphological structure Occurrence False Congenital Inferred relationship Existential restriction modifier
Posterior buccal occlusion of mandibular teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital varicella syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Curry-Hall syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Trichodental syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Laryngo-onychocutaneous syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Juvenile elastoma Occurrence False Congenital Inferred relationship Existential restriction modifier
Carbohydrate-deficient glycoprotein syndrome type I Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Carbohydrate-deficient glycoprotein syndrome type II Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Carbohydrate-deficient glycoprotein syndrome type III Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atelencephaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Aprosencephaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Schprintzen Occurrence False Congenital Inferred relationship Existential restriction modifier
Combined malformation of central nervous system and skeletal muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Muscle eye brain disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, perinatal lethal (disorder) Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypothyroidism with diffuse goiter Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Occurrence False Congenital Inferred relationship Existential restriction modifier
Atresia of nasolacrimal duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hydrocalicosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Transverse deficiency lower limb - knee level Occurrence False Congenital Inferred relationship Existential restriction modifier
Dental midlines coincident and incorrect Occurrence False Congenital Inferred relationship Existential restriction modifier
Spondylodysplastic group Occurrence False Congenital Inferred relationship Existential restriction modifier
Short rib dysplasia group (with or without polydactyly) Occurrence False Congenital Inferred relationship Existential restriction modifier
Kniest-Stickler dysplasia group Occurrence False Congenital Inferred relationship Existential restriction modifier
Spondyloepiphyseal dysplasia congenita group Occurrence False Congenital Inferred relationship Existential restriction modifier
Chondrodysplasia punctata Occurrence False Congenital Inferred relationship Existential restriction modifier
Bent bone dysplasia group Occurrence False Congenital Inferred relationship Existential restriction modifier
Craniometadiaphyseal dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Idiopathic multicentric osteolysis Occurrence False Congenital Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence False Congenital Inferred relationship Existential restriction modifier
Transient mitral regurgitation of newborn Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hepatitis C infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Sialic storage disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of nipple Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysostosis multiplex group Occurrence False Congenital Inferred relationship Existential restriction modifier
Acromesomelic dysplasia group Occurrence False Congenital Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Occurrence False Congenital Inferred relationship Existential restriction modifier
Tubule of epoophoron Occurrence False Congenital Inferred relationship Existential restriction modifier
Duct of epoophoron Occurrence False Congenital Inferred relationship Existential restriction modifier
Vesicular appendix of ovary Occurrence False Congenital Inferred relationship Existential restriction modifier
Paroophoron Occurrence False Congenital Inferred relationship Existential restriction modifier
Tubule of paroophoron Occurrence False Congenital Inferred relationship Existential restriction modifier
Venous remnant Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent descending vein Occurrence False Congenital Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV A Occurrence False Congenital Inferred relationship Existential restriction modifier
Disorder of branched-chain amino acid metabolism Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple congenital malformations Occurrence False Congenital Inferred relationship Existential restriction modifier
Arterial embryological remnant Occurrence False Congenital Inferred relationship Existential restriction modifier
Gangrenous omphalocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stricture of common bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Vestigial gastrointestinal remnant Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus of bursa co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus of tendon co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus of olecranon bursa co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus of prepatellar bursa co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Lumbarized first sacral vertebra Occurrence False Congenital Inferred relationship Existential restriction modifier
Sacralization of fifth lumbar vertebra Occurrence False Congenital Inferred relationship Existential restriction modifier
Neuromuscular kyphoscoliosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Thoracogenic kyphoscoliosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Crossed ectopia of testis Occurrence False Congenital Inferred relationship Existential restriction modifier
Pentalogy of Cantrell Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital agammaglobulinemia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital stenosis of pulmonary veins Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arterial aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of external ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of nose and nasopharynx Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of oral cavity Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of salivary duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Intercritical gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Interval gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital inversion of nipple Occurrence False Congenital Inferred relationship Existential restriction modifier
Manifest-latent nystagmus Occurrence False Congenital Inferred relationship Existential restriction modifier
Esophageal diverticulum Occurrence False Congenital Inferred relationship Existential restriction modifier
Hemicephaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Neck webbing Occurrence False Congenital Inferred relationship Existential restriction modifier
Dominant epidermolysis bullosa simplex, Weber-Cockayne type Occurrence False Congenital Inferred relationship Existential restriction modifier

Start Previous Page 22 of 343 Next End


This concept is not in any reference sets

Back to Start