Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3317076011 | Absence of fingerprints with congenital milia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3317077019 | Absence of fingerprints with congenital milia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3317078012 | Absence of dermatoglyphics with congenital milia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3317079016 | Baird syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3317080018 | This syndrome has characteristics of neonatal blisters, milia and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 874491000172111 | syndrome de Baird | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 1010721000172115 | syndrome d'absence de dermatoglyphes-miliaire congénital | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Abnormal dermatoglyphic pattern (disorder) | true | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Aplasia of skin | false | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Milia | true | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Congenital absence | false | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Associated morphology | Milium | false | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Finding site | Structure of dermatoglyphic patterns | false | Inferred relationship | Some | 3 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Finding site | Structure of dermatoglyphic patterns | true | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Associated morphology | Milium | true | Inferred relationship | Some | 1 | |
| Absence of fingerprints with congenital milia syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Absence of fingerprints with congenital milia syndrome (disorder) | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR