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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
RHYNS syndrome Occurrence True Congenital Inferred relationship Some 3
Patterson Stevenson Fontaine syndrome Occurrence True Congenital Inferred relationship Some 1
Lowry Wood syndrome Occurrence True Congenital Inferred relationship Some 2
Lowry Wood syndrome Occurrence True Congenital Inferred relationship Some 1
Aglossia-adactyly syndrome Occurrence True Congenital Inferred relationship Some 1
Vascular ring with left aortic arch and right arterial duct arising from retro-oesophageal aortic diverticulum and aberrant right subclavian artery Occurrence True Congenital Inferred relationship Some 1
Thomas syndrome Occurrence True Congenital Inferred relationship Some 1
Double mitral valve Occurrence True Congenital Inferred relationship Some 1
Fetus with central nervous system malformation unspecified Occurrence False Congenital Inferred relationship Some
Split hand, split foot malformation with sensorineural hearing loss syndrome Occurrence True Congenital Inferred relationship Some 1
Split hand, split foot malformation with sensorineural hearing loss syndrome Occurrence True Congenital Inferred relationship Some 3
Split hand, split foot malformation with sensorineural hearing loss syndrome Occurrence False Congenital Inferred relationship Some 2
Incomplete ossification of supraoccipital bone Occurrence True Congenital Inferred relationship Some 1
Multiple malformation syndrome with facial-limb defects as major feature Occurrence True Congenital Inferred relationship Some 1
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome Occurrence True Congenital Inferred relationship Some 1
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome Occurrence True Congenital Inferred relationship Some 2
Fetus with central nervous system malformation NOS Occurrence False Congenital Inferred relationship Some
Incomplete ossification of centrum of lumbar vertebra Occurrence True Congenital Inferred relationship Some 1
Pre-eruptive colour change of tooth Occurrence False Congenital Inferred relationship Some 1
Fetus with chromosomal abnormality unspecified Occurrence False Congenital Inferred relationship Some
Mesomelic dysplasia Occurrence True Congenital Inferred relationship Some 1
Trigonocephaly with bifid nose and acral anomaly syndrome Occurrence True Congenital Inferred relationship Some 1
Trigonocephaly with bifid nose and acral anomaly syndrome Occurrence True Congenital Inferred relationship Some 2
Trigonocephaly with bifid nose and acral anomaly syndrome Occurrence True Congenital Inferred relationship Some 3
Spinocerebellar ataxia type 34 Occurrence True Congenital Inferred relationship Some 1
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence False Congenital Inferred relationship Some 1
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia Occurrence True Congenital Inferred relationship Some 1
Fetus with chromosomal abnormality NOS Occurrence False Congenital Inferred relationship Some
Fetus with hereditary disease unspecified Occurrence False Congenital Inferred relationship Some
Junctional epidermolysis bullosa gravis of Herlitz Occurrence True Congenital Inferred relationship Some 1
Camptodactyly and tall stature with scoliosis and hearing loss syndrome Occurrence True Congenital Inferred relationship Some 2
Camptodactyly and tall stature with scoliosis and hearing loss syndrome Occurrence True Congenital Inferred relationship Some 1
Camptodactyly and tall stature with scoliosis and hearing loss syndrome Occurrence True Congenital Inferred relationship Some 3
L1 syndrome Occurrence True Congenital Inferred relationship Some 1
Roger's disease Occurrence True Congenital Inferred relationship Some 1
Bone dysplasia lethal Holmgren type Occurrence True Congenital Inferred relationship Some 1
Thrombocytopathy, asplenia and miosis Occurrence False Congenital Inferred relationship Some 2
Fetus with hereditary disease NOS Occurrence False Congenital Inferred relationship Some
Auricular abnormality, cleft lip, ocular abnormality syndrome Occurrence True Congenital Inferred relationship Some 2
Auricular abnormality, cleft lip, ocular abnormality syndrome Occurrence True Congenital Inferred relationship Some 1
Fetus with viral damage via mother unspecified Occurrence False Congenital Inferred relationship Some
Fucosidosis Occurrence True Congenital Inferred relationship Some 1
Brittle cornea syndrome Occurrence True Congenital Inferred relationship Some 1
Congenital postural lordosis Occurrence False Congenital Inferred relationship Some 1
Congenital hypoplasia of cardiac ventricle Occurrence True Congenital Inferred relationship Some 1
Atrioventricular septal defect - ventricular component under inferior bridging leaflet Occurrence True Congenital Inferred relationship Some 1
Absent thumb with short stature and immunodeficiency syndrome Occurrence True Congenital Inferred relationship Some 1
Absent thumb with short stature and immunodeficiency syndrome Occurrence True Congenital Inferred relationship Some 2
Persisting fifth aortic arch with atresia of fourth arch Occurrence True Congenital Inferred relationship Some 1
Congenital fistula between uterus and urinary tract Occurrence True Congenital Inferred relationship Some 1
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism Occurrence True Congenital Inferred relationship Some 1
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism Occurrence False Congenital Inferred relationship Some 2
Congenital chorioretinal degeneration Occurrence True Congenital Inferred relationship Some 1
Incomplete ossification of tarsal bone Occurrence True Congenital Inferred relationship Some 1
Fetus with viral damage via mother NOS Occurrence False Congenital Inferred relationship Some
Congenital nuclear ophthalmoplegia Occurrence True Congenital Inferred relationship Some 1
Fetus with damage due to other maternal disease unspecified Occurrence False Congenital Inferred relationship Some
Craniodiaphyseal dysplasia Occurrence True Congenital Inferred relationship Some 1
Achondrogenesis, type II Occurrence True Congenital Inferred relationship Some 1
Grebe syndrome Occurrence True Congenital Inferred relationship Some 1
Vitelline duct polyp Occurrence True Congenital Inferred relationship Some 1
Sandman-Andra syndrome Occurrence True Congenital Inferred relationship Some 1
Rolland-Debuqois syndrome Occurrence True Congenital Inferred relationship Some 1
Hypoplasia of uterus and cervix Occurrence True Congenital Inferred relationship Some 1
Fetus with damage due to other maternal disease - delivered Occurrence False Congenital Inferred relationship Some
EEM syndrome Occurrence True Congenital Inferred relationship Some 3
EEM syndrome Occurrence True Congenital Inferred relationship Some 1
EEM syndrome Occurrence True Congenital Inferred relationship Some 2
Fetus with damage due to other maternal disease with antenatal problem Occurrence False Congenital Inferred relationship Some
Supernumerary fused sternebra Occurrence True Congenital Inferred relationship Some 1
Complete bilateral cleft palate Occurrence True Congenital Inferred relationship Some 1
Complete bilateral cleft palate Occurrence True Congenital Inferred relationship Some 2
Autosomal dominant brachyolmia Occurrence False Congenital Inferred relationship Some 2
Autosomal dominant brachyolmia Occurrence True Congenital Inferred relationship Some 1
Uterus subseptus Occurrence True Congenital Inferred relationship Some 1
Inverse junctional epidermolysis bullosa Occurrence True Congenital Inferred relationship Some 1
Multiple café-au-lait macules due to neurofibromatosis Occurrence True Congenital Inferred relationship Some 1
Multiple café-au-lait macules due to neurofibromatosis Occurrence True Congenital Inferred relationship Some 2
Fetus with damage due to other maternal disease NOS Occurrence False Congenital Inferred relationship Some
Tracheal origin of right upper lobe bronchus Occurrence True Congenital Inferred relationship Some 1
Fetus with drug damage unspecified Occurrence False Congenital Inferred relationship Some
Temtamy syndrome Occurrence True Congenital Inferred relationship Some 2
Temtamy syndrome Occurrence True Congenital Inferred relationship Some 3
Uterus cordiformis Occurrence True Congenital Inferred relationship Some 1
Kartagener syndrome Occurrence True Congenital Inferred relationship Some 2
Bilateral renal dysplasia Occurrence True Congenital Inferred relationship Some 1
Polyvalvular heart disease syndrome Occurrence True Congenital Inferred relationship Some 1
Complete situs inversus with dextrocardia Occurrence True Congenital Inferred relationship Some 1
Thanatophoric dysplasia, type 2 Occurrence True Congenital Inferred relationship Some 1
Congenital pericardial defect Occurrence True Congenital Inferred relationship Some 1
Fetus with drug damage NOS Occurrence False Congenital Inferred relationship Some
Dysplasias with significant membranous bone involvement Occurrence True Congenital Inferred relationship Some 1
Fetus with radiation damage unspecified Occurrence False Congenital Inferred relationship Some
Mononen Karnes Senac syndrome Occurrence True Congenital Inferred relationship Some 1
Branchial cleft, cyst or fistula; preauricular sinus Occurrence False Congenital Inferred relationship Some 1
Holoprosencephaly and postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Some 1
Short tarsus with absence of lower eyelashes syndrome Occurrence True Congenital Inferred relationship Some 1
Congenital pulmonary artery conduit Occurrence True Congenital Inferred relationship Some 1
Right renal agenesis co-occurrent with left renal hypoplasia Occurrence True Congenital Inferred relationship Some 1
Smith McCort dysplasia Occurrence True Congenital Inferred relationship Some 1
Radioulnar synostosis with microcephaly and scoliosis syndrome Occurrence True Congenital Inferred relationship Some 1

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Reference Sets

Qualifier value foundation reference set

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