Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304697013 | Holoprosencephaly and postaxial polydactyly syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304698015 | Holoprosencephaly and postaxial polydactyly syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304699011 | Pseudotrisomy 13 syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401215011 | Holoprosencephaly-postaxial polydactyly syndrome associates, in chromosomally normal neonates, holoprosencephaly, severe facial dysmorphism, postaxial polydactyly and other congenital abnormalities, suggestive of trisomy 13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Is a | Holoprosencephaly sequence | true | Inferred relationship | Some | ||
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Is a | Polydactyly (disorder) | true | Inferred relationship | Some | ||
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Associated morphology | Supernumerary structure | false | Inferred relationship | Some | 3 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Finding site | Digit structure | false | Inferred relationship | Some | 3 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 1 | |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)