Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3315795011 | Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3315799017 | Primary hypergonadotropic hypogonadism and partial alopecia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3315800018 | Al Awadi Farag Teebi syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Partial loss of hair | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Hereditary disorder of the integument | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Primary hypogonadism | true | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Finding site | Gonadal endocrine structure | false | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Associated morphology | Absence | false | Inferred relationship | Existential restriction modifier | 2 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Finding site | Hair structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Associated morphology | Absence | true | Inferred relationship | Existential restriction modifier | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Finding site | Hair structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 3 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Finding site | Gonadal endocrine structure | false | Inferred relationship | Existential restriction modifier | 3 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | Congenital disease | false | Inferred relationship | Existential restriction modifier | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR