Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3429754015 | Polysyndactyly and cardiac malformation syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429755019 | Polysyndactyly and cardiac malformation syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429756018 | Bonneau syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403208014 | A rare, life-threatening developmental defect during embryogenesis characterized by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403209018 | A rare, life-threatening developmental defect during embryogenesis characterised by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Congenital heart disease | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Polysyndactyly (disorder) | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Finding site | Heart structure | false | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Congenital abnormal fusion | false | Inferred relationship | Some | 3 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 3 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Congenital abnormal fusion | false | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Supernumerary structure | false | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Finding site | Digit structure | false | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 3 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Finding site | Heart structure | true | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Polysyndactyly and cardiac malformation syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Polysyndactyly and cardiac malformation syndrome (disorder) | Associated morphology | Abnormally fused structure (morphologic abnormality) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)