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255399007: Congenital (qualifier value)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Case insensitive SNOMED CT core
380599019 Congenita en Synonym Active Case insensitive SNOMED CT core
646433016 Congenital (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Trigonocephaly with broad thumb syndrome Occurrence True Congenital Inferred relationship Some 4
Trigonocephaly with broad thumb syndrome Occurrence True Congenital Inferred relationship Some 2
Trigonocephaly with broad thumb syndrome Occurrence True Congenital Inferred relationship Some 3
Cerebellum agenesis with hydrocephaly Occurrence True Congenital Inferred relationship Some 1
Congenital arteriovenous malformation of small intestine Occurrence True Congenital Inferred relationship Some 1
Faun tail syndrome Occurrence False Congenital Inferred relationship Some 2
Weismann Netter syndrome Occurrence True Congenital Inferred relationship Some 1
Neurofibromatosis type 1 Occurrence True Congenital Inferred relationship Some 2
Inherited arthrogryposis Occurrence True Congenital Inferred relationship Some 1
Kyphomelic dysplasia Occurrence True Congenital Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Occurrence True Congenital Inferred relationship Some 1
Absence deformity of leg and congenital cataract syndrome Occurrence True Congenital Inferred relationship Some 1
Penile shaft hypospadias Occurrence True Congenital Inferred relationship Some 1
Oculoauriculovertebral spectrum with radial defects Occurrence True Congenital Inferred relationship Some 1
Cleft palate with left cleft lip Occurrence True Congenital Inferred relationship Some 1
Coffin-Lowry syndrome Occurrence True Congenital Inferred relationship Some 2
Bipartite ossification of centrum of sacral vertebra Occurrence True Congenital Inferred relationship Some 1
Retinal arteriovenous shunt Occurrence True Congenital Inferred relationship Some 1
MacDermot Winter syndrome Occurrence True Congenital Inferred relationship Some 1
Adams-Oliver syndrome Occurrence True Congenital Inferred relationship Some 1
Systemic to coronary collateral artery Occurrence True Congenital Inferred relationship Some 2
Congenital spinal meningocele Occurrence True Congenital Inferred relationship Some 1
Congenital spinal meningocele Occurrence True Congenital Inferred relationship Some 2
Dystrophic epidermolysis bullosa nails only Occurrence True Congenital Inferred relationship Some 1
Dystrophic epidermolysis bullosa nails only Occurrence True Congenital Inferred relationship Some 2
Osteopathia striata with cranial sclerosis Occurrence True Congenital Inferred relationship Some 1
Dual coronary orifice Occurrence True Congenital Inferred relationship Some 1
Congenital abnormality of atrioventricular valve leaflet in atrioventricular septal defect Occurrence True Congenital Inferred relationship Some 1
Porokeratosis of Mibelli, linear unilateral type Occurrence False Congenital Inferred relationship Some 1
Cutis laxa, autosomal recessive Occurrence True Congenital Inferred relationship Some 1
Blepharoptosis, myopia, ectopia lentis syndrome Occurrence True Congenital Inferred relationship Some 1
Kirman syndrome Occurrence True Congenital Inferred relationship Some 1
Craniomicromelic syndrome Occurrence True Congenital Inferred relationship Some 3
Craniomicromelic syndrome Occurrence True Congenital Inferred relationship Some 1
Craniomicromelic syndrome Occurrence True Congenital Inferred relationship Some 2
Pontocerebellar hypoplasia type 4 Occurrence True Congenital Inferred relationship Some 1
Persistent cloaca Occurrence True Congenital Inferred relationship Some 2
Persistent cloaca Occurrence True Congenital Inferred relationship Some 1
Congenital absence of oesophagus with tracheo-oesophageal fistula Occurrence True Congenital Inferred relationship Some 2
Incomplete ossification of clavicle Occurrence True Congenital Inferred relationship Some 1
Congenital anomalies of ovaries and fallopian tubes Occurrence True Congenital Inferred relationship Some 2
Congenital anomalies of ovaries and fallopian tubes Occurrence True Congenital Inferred relationship Some 1
Intractable diarrhoea with choanal atresia and eye anomaly syndrome Occurrence True Congenital Inferred relationship Some 3
Intractable diarrhoea with choanal atresia and eye anomaly syndrome Occurrence True Congenital Inferred relationship Some 2
Intractable diarrhoea with choanal atresia and eye anomaly syndrome Occurrence True Congenital Inferred relationship Some 1
Patent urachus Occurrence True Congenital Inferred relationship Some 1
Bent bone dysplasia group Occurrence True Congenital Inferred relationship Some 1
Polysomia Occurrence True Congenital Inferred relationship Some 1
Lingual ectopic tooth Occurrence False Congenital Inferred relationship Some 1
Anonychia with bizarre flexural pigmentation Occurrence True Congenital Inferred relationship Some 1
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth Occurrence True Congenital Inferred relationship Some 2
Aortico-left ventricular tunnel with aneurysm of intracardiac septal wall and aneurysm of extracardiac aortic wall Occurrence True Congenital Inferred relationship Some 1
Aortico-left ventricular tunnel with aneurysm of intracardiac septal wall and aneurysm of extracardiac aortic wall Occurrence True Congenital Inferred relationship Some 2
Subpulmonary infundibulum Occurrence True Congenital Inferred relationship Some 1
Oculodentodigital syndrome Occurrence True Congenital Inferred relationship Some 3
Acephalogaster Occurrence True Congenital Inferred relationship Some 1
Autosomal recessive cerebelloparenchymal disorder type 3 Occurrence True Congenital Inferred relationship Some 1
Eyebrow duplication syndactyly syndrome Occurrence True Congenital Inferred relationship Some 1
Eyebrow duplication syndactyly syndrome Occurrence True Congenital Inferred relationship Some 2
Tuberous sclerosis syndrome Occurrence True Congenital Inferred relationship Some 1
Hydromyelocele with hydrocephalus Occurrence False Congenital Inferred relationship Some 3
Congenital extrahepatic portal-systemic shunt Occurrence True Congenital Inferred relationship Some 1
Midline cervical cleft Occurrence True Congenital Inferred relationship Some 1
Odontochondrodysplasia Occurrence True Congenital Inferred relationship Some 1
Odontochondrodysplasia Occurrence True Congenital Inferred relationship Some 2
Agnathia, holoprosencephaly, situs inversus syndrome Occurrence True Congenital Inferred relationship Some 1
Osseous syndactyly lesser toes Occurrence True Congenital Inferred relationship Some 1
Multiple epiphyseal dysplasia Al-Gazali type Occurrence True Congenital Inferred relationship Some 1
Ectopic pancreas in duodenum Occurrence True Congenital Inferred relationship Some 1
Crowding of anterior mandibular teeth Occurrence False Congenital Inferred relationship Some 2
Microphakia Occurrence True Congenital Inferred relationship Some 1
Constriction ring of upper limb with lymphoedema Occurrence True Congenital Inferred relationship Some 1
Wolf Hirschhorn syndrome Occurrence True Congenital Inferred relationship Some 1
Small intestine atresia and stenosis Occurrence True Congenital Inferred relationship Some 1
Incomplete ossification of ulna Occurrence True Congenital Inferred relationship Some 1
Septoparietal trabeculations Occurrence True Congenital Inferred relationship Some 1
Harrod syndrome Occurrence True Congenital Inferred relationship Some 1
Harrod syndrome Occurrence True Congenital Inferred relationship Some 3
Harrod syndrome Occurrence True Congenital Inferred relationship Some 2
Trichodysplasia with amelogenesis imperfecta syndrome Occurrence True Congenital Inferred relationship Some 2
Trichodysplasia with amelogenesis imperfecta syndrome Occurrence True Congenital Inferred relationship Some 1
Ectodermal dysplasia with nail defect Occurrence True Congenital Inferred relationship Some 1
Congenital koilonychia Occurrence True Congenital Inferred relationship Some 1
Iniencephaly Occurrence True Congenital Inferred relationship Some 2
Ear auricle and external auditory canal absent Occurrence True Congenital Inferred relationship Some 1
Penile mid-shaft hypospadias Occurrence True Congenital Inferred relationship Some 1
Combined malformation of central nervous system and skeletal muscle Occurrence True Congenital Inferred relationship Some 1
Syringomyelobulbia Occurrence True Congenital Inferred relationship Some 1
Elephantiasis neurofibromatosa Occurrence True Congenital Inferred relationship Some 2
Elephantiasis neurofibromatosa Occurrence True Congenital Inferred relationship Some 1
Triphalangeal thumb and polysyndactyly syndrome Occurrence True Congenital Inferred relationship Some 1
Crane Heise syndrome Occurrence True Congenital Inferred relationship Some 2
Crane Heise syndrome Occurrence True Congenital Inferred relationship Some 1
Dominant dystrophic epidermolysis bullosa Occurrence True Congenital Inferred relationship Some 1
Congenital laryngomalacia Occurrence True Congenital Inferred relationship Some 1
Duplex ureter structure Occurrence False Congenital Inferred relationship Some 1
Pili torti onychodysplasia syndrome Occurrence True Congenital Inferred relationship Some 1
Pili torti onychodysplasia syndrome Occurrence True Congenital Inferred relationship Some 3
Pili torti onychodysplasia syndrome Occurrence True Congenital Inferred relationship Some 2
Craniopagus frontalis Occurrence True Congenital Inferred relationship Some 1
Sponastrime dysplasia Occurrence True Congenital Inferred relationship Some 1

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Reference Sets

Qualifier value foundation reference set

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