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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
Osteogenesis imperfecta, dominant perinatal lethal Occurrence False Congenital Inferred relationship Existential restriction modifier
Absent finger Occurrence False Congenital Inferred relationship Existential restriction modifier
Dipygus Occurrence False Congenital Inferred relationship Existential restriction modifier
Celoschisis Occurrence False Congenital Inferred relationship Existential restriction modifier
Macrodontia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital supravalvular aortic stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Maple syrup urine disease, multiple dehydrogenase form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Complete trisomy 22 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Lysinuric protein intolerance, type 2 Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked hydrocephalus syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Anophthalmos Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital contracted pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent class II human leukocyte antigens Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital anomaly of broad ligament Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital aplasia of inner ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Aase syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Tuberous sclerosis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Abnormal fetal duplication Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital deformity of nose Occurrence False Congenital Inferred relationship Existential restriction modifier
Long narrow head Occurrence False Congenital Inferred relationship Existential restriction modifier
Postductal coarctation of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypoplasia of cardiac vein Occurrence False Congenital Inferred relationship Existential restriction modifier
Inborn error of glutathione metabolism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of larynx Occurrence False Congenital Inferred relationship Existential restriction modifier
Bicuspid aortic valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of diaphragm Occurrence False Congenital Inferred relationship Existential restriction modifier
Bilateral left-sidedness sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Niemann-Pick disease, type C, chronic form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked ichthyosis with steryl-sulfatase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Cervical rib Occurrence False Congenital Inferred relationship Existential restriction modifier
Hydroxymethylglutaryl-CoA lyase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis IV-A Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Uterus bicornis bicollis Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogen storage disease, type I Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Isolated xanthine oxidase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Gronblad-Strandberg syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Vitamin D-dependent rickets, type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital prognathism Occurrence False Congenital Inferred relationship Existential restriction modifier
Megaloappendix Occurrence False Congenital Inferred relationship Existential restriction modifier
Moore-Federman syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Short rib-polydactyly syndrome, Majewski type Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cystic disease of liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Kynureninase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of epiglottis Occurrence False Congenital Inferred relationship Existential restriction modifier
Gastroschisis Occurrence False Congenital Inferred relationship Existential restriction modifier
Polyploidy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Thoracogenic scoliosis Occurrence False Congenital Inferred relationship Existential restriction modifier
10q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Coarctation of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis type I-S Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hunter's syndrome, severe form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pena-Shokeir phenotype Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory adrenal cortex Occurrence False Congenital Inferred relationship Existential restriction modifier
Mousepox Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of the urinary system Occurrence False Congenital Inferred relationship Existential restriction modifier
Marshall-Smith syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of parathyroid gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Hemimyelia Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Niemann-Pick disease, type E Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Opocephalus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of germinal epithelium of testes Occurrence False Congenital Inferred relationship Existential restriction modifier
Adolescent postural kyphosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of musculoskeletal system Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital subaortic stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Neurologic xeroderma pigmentosum Occurrence False Congenital Inferred relationship Existential restriction modifier
Double outlet left ventricle Occurrence False Congenital Inferred relationship Existential restriction modifier
Common arterial trunk and common origin of pulmonary arteries Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cutaneous angiomatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Cobalamin A disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Adult GM>1< gangliosidosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa with osteodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Metabolic disease of collagen Occurrence False Congenital Inferred relationship Existential restriction modifier
Perinatal jaundice due to inspissated bile syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Chronic tophaceous gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital toxoplasmosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malposition of digestive organs Occurrence False Congenital Inferred relationship Existential restriction modifier
Partial trisomy of short arm of chromosome 5 Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of pituitary gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Isolated dextrocardia Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebellar hemangioblastomatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Progressive intrahepatic cholestasis Occurrence False Congenital Inferred relationship Existential restriction modifier
Partial tetrasomy of chromosome 9 Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery arising from main pulmonary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital scar Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of fibula Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary coproporphyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Female infertility due to structural congenital anomaly of cervix Occurrence False Congenital Inferred relationship Existential restriction modifier
Opodidymus Occurrence False Congenital Inferred relationship Existential restriction modifier
Woolf's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital disorder due to abnormality of chromosome number OR structure Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete trisomy 9 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Micromelia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Manus flexa Occurrence False Congenital Inferred relationship Existential restriction modifier
XX males Occurrence False Congenital Inferred relationship Existential restriction modifier
Craniopagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Kommerell's diverticulum Occurrence False Congenital Inferred relationship Existential restriction modifier
Diplopodia Occurrence False Congenital Inferred relationship Existential restriction modifier
Crossed renal ectopia Occurrence False Congenital Inferred relationship Existential restriction modifier

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