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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
Prion disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant variant form of albumin Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked absence of thyroxine-binding globulin Occurrence False Congenital Inferred relationship Existential restriction modifier
Iodide transport defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Iodotyrosyl coupling defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis marmorata Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fiber type disproportion myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Floppy infant syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Zebra body myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Inherited disorder of thyroid metabolism Occurrence False Congenital Inferred relationship Existential restriction modifier
Chronic wasting disease of captive mule deer AND/OR elk Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked reduction of thyroxine-binding globulin Occurrence False Congenital Inferred relationship Existential restriction modifier
Central core disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Sarcotubular myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroglobulin proteolysis defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Severe X-linked myotubular myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Angioma serpiginosum Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroid hormone responsiveness defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Iodide oxidation defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Pigmented hairy epidermal nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital muscular hypertrophy-cerebral syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Multi-core congenital myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked excess of thyroxine-binding globulin Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypothyroidism due to defect in thyroid hormone synthesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Facioscapulohumeral muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroxine transport defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Distal muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroglobulin synthesis defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Myxedematous form of cretinism Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant excess of transthyretin Occurrence False Congenital Inferred relationship Existential restriction modifier
Gerstmann-Straussler-Scheinker syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Mixed congenital myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital myopathy with abnormal subcellular organelles Occurrence False Congenital Inferred relationship Existential restriction modifier
Pendred's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Nevus unius lateris Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked variant form of thyroxine-binding globulin Occurrence False Congenital Inferred relationship Existential restriction modifier
Transmissible mink encephalopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Nemaline myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Duchenne muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Oculopharyngeal muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroxine plasma membrane transport defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Iodide peroxidase defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Myotubular myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Fatal familial insomnia Occurrence False Congenital Inferred relationship Existential restriction modifier
Progressive subcortical gliosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Single supernumerary tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Arteriovenous malformation of kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive severe combined immunodeficiency disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Malignant neoplasm of Gartner's duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital and developmental myasthenia Occurrence False Congenital Inferred relationship Existential restriction modifier
Atrial septal defect due to and following acute myocardial infarction Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital aneurysm of heart Occurrence False Congenital Inferred relationship Existential restriction modifier
Lithopedian Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired hemangiomatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Nemaline myopathy, early onset type Occurrence False Congenital Inferred relationship Existential restriction modifier
Nemaline myopathy, late onset type Occurrence False Congenital Inferred relationship Existential restriction modifier
[X]Dementia in Creutzfeldt-Jakob disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary edema of legs NOS Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arthrogryposis caused by teratogen Occurrence False Congenital Inferred relationship Existential restriction modifier
Hepatoportal microvascular dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Schistosomus reflexus Occurrence False Congenital Inferred relationship Existential restriction modifier
Mittendorf's dot Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of endocrine ovary Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of both testes Occurrence False Congenital Inferred relationship Existential restriction modifier
Translocation Down syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital syringomyelia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital leg length discrepancy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of endocrine gonad Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of endocrine testis Occurrence False Congenital Inferred relationship Existential restriction modifier
Bilateral acheiria Occurrence False Congenital Inferred relationship Existential restriction modifier
Bilateral congenital absence of feet Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of hand Occurrence False Congenital Inferred relationship Existential restriction modifier
Unilateral acheiria Occurrence False Congenital Inferred relationship Existential restriction modifier
Unilateral congenital absence of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Porphyrinopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital dislocation of elbow Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery fistula to left atrium Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery fistula to left ventricle Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery fistula to right atrium Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery fistula to right ventricle Occurrence False Congenital Inferred relationship Existential restriction modifier
Syndactyly Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital bony fusion of phalanges Occurrence False Congenital Inferred relationship Existential restriction modifier
Bovine hereditary syndactyly Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital obstruction of ureteropelvic junction Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital obstruction of ureteral orifice Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital urinary meatus obstruction Occurrence False Congenital Inferred relationship Existential restriction modifier
Chiari malformation type II Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital vesicoureterorenal reflux Occurrence False Congenital Inferred relationship Existential restriction modifier
Cleft lip and cleft of alveolar process of maxilla Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypoplasia of optic disc Occurrence False Congenital Inferred relationship Existential restriction modifier
Optic disc hypoplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Optic disc structural anomaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital pancreatic enterokinase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital spondylolisthesis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of vertebra Occurrence False Congenital Inferred relationship Existential restriction modifier
Sacralization of lumbar vertebra Occurrence False Congenital Inferred relationship Existential restriction modifier

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