Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3706553013 | X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
3706554019 | IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3706555018 | X-linked central congenital hypothyroidism with late-onset macroorchidism | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3706556017 | X-linked central congenital hypothyroidism with late-onset testicular enlargement | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Associated morphology | Hypertrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Finding site | Thyroid structure | true | Inferred relationship | Existential restriction modifier | 2 | |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Occurrence | Adolescence | true | Inferred relationship | Existential restriction modifier | 1 | |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | Central hypothyroidism | true | Inferred relationship | Existential restriction modifier | ||
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | X-linked hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Finding site | Testis structure | true | Inferred relationship | Existential restriction modifier | 1 | |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | Hypertrophy of testis | true | Inferred relationship | Existential restriction modifier | ||
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets