Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2983485017 | WNT4 Mullerian aplasia and ovarian dysfunction | en | Synonym | Active | Case sensitive | SNOMED CT core |
2983507013 | Biason-Lauber syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
2983526017 | WNT4 protein deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
2983527014 | Mayer-Rokitansky-Küster-Hausel like syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
2988285017 | WNT4 Müllerian aplasia and ovarian dysfunction (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3014902017 | WNT4 Müllerian aplasia and ovarian dysfunction | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
WNT4 Mullerian aplasia and ovarian dysfunction | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Associated morphology | Agenesis | false | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Structure of paramesonephric duct | true | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Associated morphology | Aplasia | true | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Is a | Mullerian aplasia | true | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Is a | Ovarian dysfunction | true | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Occurrence | Congenital | false | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Ovarian endocrine structure | false | Inferred relationship | Some | ||
WNT4 Mullerian aplasia and ovarian dysfunction | Associated morphology | Congenital absence | false | Inferred relationship | Some | 3 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Uterine structure | false | Inferred relationship | Some | 3 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Uterine structure | false | Inferred relationship | Some | 1 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Associated morphology | Congenital absence | false | Inferred relationship | Some | 1 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Associated morphology | Congenital absence | false | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Entire uterus | false | Inferred relationship | Some | 2 | |
WNT4 Mullerian aplasia and ovarian dysfunction | Finding site | Ovarian endocrine structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set