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
Congenital anomaly of peripheral nerve Occurrence False Congenital Inferred relationship Existential restriction modifier
Achondrogenesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic splenic tissue Occurrence False Congenital Inferred relationship Existential restriction modifier
Imperfect fusion of skull Occurrence False Congenital Inferred relationship Existential restriction modifier
Funicular hernia of umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomaly of dental arch Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperleucinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Median mandibular cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete bilateral cleft palate Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Occurrence False Congenital Inferred relationship Existential restriction modifier
Distal arthrogryposis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dilatation of colon Occurrence False Congenital Inferred relationship Existential restriction modifier
Xiphopagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Cystathionine beta-synthase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Metachromatic leukodystrophy, adult type Occurrence False Congenital Inferred relationship Existential restriction modifier
Meromicrosomia Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory thymic tissue Occurrence False Congenital Inferred relationship Existential restriction modifier
Iniencephaly Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Thoracodelphus Occurrence False Congenital Inferred relationship Existential restriction modifier
Mutilating keratoderma Occurrence False Congenital Inferred relationship Existential restriction modifier
Primary gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory eyelid Occurrence False Congenital Inferred relationship Existential restriction modifier
Laterality sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Posterior open bite Occurrence False Congenital Inferred relationship Existential restriction modifier
Metaphyseal chondrodysplasia, Jansen type Occurrence False Congenital Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class III variant anemia Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Thoracopagus parasiticus Occurrence False Congenital Inferred relationship Existential restriction modifier
Townes syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Infantile cortical hyperostosis Occurrence False Congenital Inferred relationship Existential restriction modifier
7p partial monosomy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of broad ligament Occurrence False Congenital Inferred relationship Existential restriction modifier
Potter's facies Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital postural lordosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cerebral arteriovenous aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of sternocleidomastoid muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Occurrence False Congenital Inferred relationship Existential restriction modifier
Benign adult cystinosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Hydromeningocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of uvula Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Coalition of calcaneus Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to spectrin deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of phalanges of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Uterus parvicollis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of vena cava Occurrence False Congenital Inferred relationship Existential restriction modifier
Phytanic acid storage disease Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Aqueduct of Sylvius anomaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Primordial cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive glutaric aciduria, type 2 Occurrence False Congenital Inferred relationship Existential restriction modifier 1
X chromosome-linked pyridoxine responsive sideroblastic anemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of left pulmonary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Syndactyly of fingers with fusion of bones Occurrence False Congenital Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome, hydroxylysine-deficient Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duodenal obstruction due to malrotation of intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fissure of sternum Occurrence False Congenital Inferred relationship Existential restriction modifier
Isolated cystinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperhydroxyprolinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Neonatal iminoglycinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Xeroderma pigmentosum, group C Occurrence False Congenital Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Chiari's network Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of ileum Occurrence False Congenital Inferred relationship Existential restriction modifier
Dubowitz's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of rectum Occurrence False Congenital Inferred relationship Existential restriction modifier
Bone island Occurrence False Congenital Inferred relationship Existential restriction modifier
Maroteaux-Lamy syndrome, intermediate form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital absence of external auditory canal Occurrence False Congenital Inferred relationship Existential restriction modifier
Microcornea Occurrence False Congenital Inferred relationship Existential restriction modifier
5-Oxoprolinase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Complete transposition of great vessels Occurrence False Congenital Inferred relationship Existential restriction modifier
Disorder: ectopic bone tissue, congenital Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of esophagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Frog fetus Occurrence False Congenital Inferred relationship Existential restriction modifier
Aortic left ventricular tunnel Occurrence False Congenital Inferred relationship Existential restriction modifier
Senter syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Chronic granulomatous disease, type IIA Occurrence False Congenital Inferred relationship Existential restriction modifier
Uterus incudiformis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital obstruction of small intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Tyrosinase-positive oculocutaneous albinism Occurrence False Congenital Inferred relationship Existential restriction modifier
Ocular albinism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital tracheocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type III Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Agyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Cat eye syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
11p partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Faun tail syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Congenital ectropion Occurrence False Congenital Inferred relationship Existential restriction modifier
Syringobulbia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of part of brain Occurrence False Congenital Inferred relationship Existential restriction modifier
Anodontia Occurrence False Congenital Inferred relationship Existential restriction modifier
Robinson nail dystrophy-deafness syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent thyroglossal duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis type I-H/S Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Coarctation of pulmonary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of superior vena cava Occurrence False Congenital Inferred relationship Existential restriction modifier
Cervical auricle Occurrence False Congenital Inferred relationship Existential restriction modifier
Dominant dystrophic epidermolysis bullosa with absence of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary ostium stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Anterior crossbite Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier

Start Previous Page 29 of 343 Next End


This concept is not in any reference sets

Back to Start