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 |
3433517012 | Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433518019 | Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433519010 | Ichthyosis, hypotrichosis, sclerosing cholangitis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433520016 | NISCH (neonatal ichthyosis, sclerosing cholangitis, hypotrichosis) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3433521017 | NISCH syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3433522012 | A very rare complex ichthyosis syndrome with characteristics of scalp hypotrichosis, scarring alopecia, ichthyosis and sclerosing cholangitis. The ichthyosis presents with diffuse white scales sparing the skin folds and is accompanied by scalp hypotrichosis, cicatricial alopecia, and sparse eyelashes/eyebrows. Additional manifestations may include oligodontia, hypodontia and enamel dysplasia. All patients present with neonatal sclerosing cholangitis with jaundice and pruritus, hepatomegaly and biochemical cholestasis. Caused by a mutation in the CLDN1 gene on chromosome 3q28 coding for the tight junction protein claudin-1. Autosomal recessive pattern of inheritance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5486881000241114 | syndrome néonatal d'ichtyose, hypotrichose et cholangite sclérosante | 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 |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Congenital hypotrichia | true | Inferred relationship | Some | ||
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Sclerosing cholangitis | true | Inferred relationship | Some | ||
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Autosomal recessive ichthyosis (disorder) | true | Inferred relationship | Some | ||
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | Congenital hypoplasia | false | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | false | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 4 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | inflammation | false | Inferred relationship | Some | 5 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Biliary tract structure | true | Inferred relationship | Some | 5 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Congenital abnormality of liver and/or biliary tract (disorder) | false | Inferred relationship | Some | ||
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 2 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | inflammation | false | Inferred relationship | Some | 1 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Biliary tract structure | true | Inferred relationship | Some | 1 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 4 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 4 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | Sclerosing inflammation | true | Inferred relationship | Some | 5 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 3 | |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) | Is a | Congenital anomaly of biliary tract | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets