Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
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 (core metadata concept) | SNOMED CT core |
3706554019 | IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706555018 | X-linked central congenital hypothyroidism with late-onset macroorchidism | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706556017 | X-linked central congenital hypothyroidism with late-onset testicular enlargement | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706557014 | A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706553013 | X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706554019 | IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706555018 | X-linked central congenital hypothyroidism with late-onset macroorchidism | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706556017 | X-linked central congenital hypothyroidism with late-onset testicular enlargement | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706557014 | A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
1052961000195114 | X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrösserung | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
895481000172117 | hypothyroïdie congénitale centrale avec macroorchidie tardive liée à l'X | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
955521000172117 | syndrome par déficit en IGSF1 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
895481000172117 | hypothyroïdie congénitale centrale avec macroorchidie tardive liée à l'X | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
955521000172117 | syndrome par déficit en IGSF1 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1052961000195114 | X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrösserung | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3397351001000119 | X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrößerung | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets