Status: current. Date: 30-Sep 2021
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4592775017 | X-linked recessive hereditary disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4592776016 | X-linked recessive hereditary disease (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked recessive hereditary disease | Is a | Hereditary disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Mucopolysaccharidosis, MPS-II | Is a | True | X-linked recessive hereditary disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Ferro-cerebro-cutaneous syndrome | Is a | True | X-linked recessive hereditary disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Contiguous ABCD1 DXS1357E deletion syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Glycogen storage disease due to muscle phosphorylase kinase deficiency (disorder) | Is a | True | X-linked recessive hereditary disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR