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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
Irido-corneal dysgenesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple malformation syndrome with facial defects as major feature Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital spinal meningocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic spleen Occurrence False Congenital Inferred relationship Existential restriction modifier
Deventer's pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory thyroid gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of parathyroid glands Occurrence False Congenital Inferred relationship Existential restriction modifier
Imidazole aminoaciduria Occurrence False Congenital Inferred relationship Existential restriction modifier
Mucopolysaccharidosis type I-H Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectopic pituitary tissue Occurrence False Congenital Inferred relationship Existential restriction modifier
Adrenoleukodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Sitosterolemia with xanthomatosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Nasal encephalocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Primary hyperoxaluria, type I Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mannosidosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Amino acid deficiency anemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Buphthalmos with megalocornea Occurrence False Congenital Inferred relationship Existential restriction modifier
High assimilation pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of cerebrovascular system Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperextension deformity of knee Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of vulva Occurrence False Congenital Inferred relationship Existential restriction modifier
Reniform pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Pseudo-Hurler polydystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Adenine phosphoribosyltransferase deficiency, Japanese type Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked agammaglobulinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Imperforate hymen Occurrence False Congenital Inferred relationship Existential restriction modifier
Bayonet hair Occurrence False Congenital Inferred relationship Existential restriction modifier
Cleidocranial dysostosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetal aminopterin syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fold of posterior segment of eye Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent hyperlysinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Miller syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Regional odontodysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of lower limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital syphilitic epiphysitis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital fusion of ribs Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperplasia of pancreatic islet beta cell Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of toe Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetal trimethadione syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cardiovascular disorder in mother complicating pregnancy, childbirth AND/OR puerperium Occurrence False Congenital Inferred relationship Existential restriction modifier
Vascular ring of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Craniopagus parietalis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of lung Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cortical cataract Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of upper limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of cerebroside-sulfatase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital cervicoaural fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Triploidy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Anadidymus Occurrence False Congenital Inferred relationship Existential restriction modifier
Cystathioninemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Mesotaurodontism Occurrence False Congenital Inferred relationship Existential restriction modifier
Niemann-Pick disease, type C Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Acrodysostosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Popliteal pterygium syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of alimentary tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomalous pulmonary venous drainage to superior vena cava Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duplication of esophagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of patella Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogen storage disease, type III Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cleft palate with cleft lip Occurrence False Congenital Inferred relationship Existential restriction modifier
18q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital lobar emphysema Occurrence False Congenital Inferred relationship Existential restriction modifier
Pyloric antral atresia Occurrence False Congenital Inferred relationship Existential restriction modifier
Vitamin D-dependent rickets, type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome, type 5 Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic pancreas in duodenum Occurrence False Congenital Inferred relationship Existential restriction modifier
Sirenoform monster Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stenosis of pulmonary valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Anterior open bite Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebral-retinal arteriovenous aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Erythropoietic porphyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Cytochrome-c oxidase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Shell teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Umbilical hernia with gangrene Occurrence False Congenital Inferred relationship Existential restriction modifier
Ichthyosis hystrix Occurrence False Congenital Inferred relationship Existential restriction modifier
Spina bifida Occurrence False Congenital Inferred relationship Existential restriction modifier 5
Pretibial epidermolysis bullosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Port-wine stain of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Tongue tie Occurrence False Congenital Inferred relationship Existential restriction modifier
Pili torti-deafness syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Aminomethyltransferase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Maroteaux-Lamy syndrome, mild form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Niemann-Pick disease, type C, subacute form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital obstruction of aqueduct of Sylvius Occurrence False Congenital Inferred relationship Existential restriction modifier
Dwarf pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Lhermitte-Duclos disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of membranous labyrinth Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of cartilage Occurrence False Congenital Inferred relationship Existential restriction modifier
Crigler-Najjar syndrome, type II Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anomalous origin of pulmonary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypoplasia of bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Partial anomalous pulmonary venous connection Occurrence False Congenital Inferred relationship Existential restriction modifier
Talipes equinovalgus Occurrence False Congenital Inferred relationship Existential restriction modifier
Vitamin D-dependent rickets Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory adrenal gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hemivertebra Occurrence False Congenital Inferred relationship Existential restriction modifier
Sphingolipid activator protein 1 deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier

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