Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2023. Module: SNOMED CT core
Descriptions:
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder) | Is a | X-linked hereditary disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Rett syndrome | Is a | True | Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder) | Inferred relationship | Some | |
| MECP2 duplication syndrome | Is a | True | Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder) | Inferred relationship | Some | |
| PPM-X syndrome | Is a | True | Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder) | Inferred relationship | Some | |
| Severe neonatal onset encephalopathy with microcephaly (disorder) | Is a | True | Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder) | Inferred relationship | Some |
This concept is not in any reference sets