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 |
| 3482379014 | Familial male-limited precocious puberty (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3482380012 | Familial male-limited precocious puberty | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3482381011 | Familial gonadotropin-independent male-limited sexual precocity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3482382016 | Familial testotoxicosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3482383014 | Male-limited precocious puberty | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403447013 | Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, early development of secondary sexual characteristics and reduced adult height. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial male-limited precocious puberty (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Is a | Precocious puberty (disorder) | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Is a | Disorder of endocrine testis | false | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Is a | Increased hormone production | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Interprets | Evaluation procedure (procedure) | false | Inferred relationship | Some | 1 | |
| Familial male-limited precocious puberty (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 3 | |
| Familial male-limited precocious puberty (disorder) | Interprets | Hormone production | true | Inferred relationship | Some | 3 | |
| Familial male-limited precocious puberty (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
| Familial male-limited precocious puberty (disorder) | Finding site | Testicular endocrine structure | false | Inferred relationship | Some | 4 | |
| Familial male-limited precocious puberty (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Familial male-limited precocious puberty (disorder) | Interprets | Endocrine observable | false | Inferred relationship | Some | 1 | |
| Familial male-limited precocious puberty (disorder) | Is a | Congenital anomaly of endocrine testis (disorder) | true | Inferred relationship | Some | ||
| Familial male-limited precocious puberty (disorder) | Finding site | Testicular endocrine structure | true | Inferred relationship | Some | 2 | |
| Familial male-limited precocious puberty (disorder) | Associated morphology | Maturation acceleration | true | Inferred relationship | Some | 2 | |
| Familial male-limited precocious puberty (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Familial male-limited precocious puberty (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR