Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3431514010 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
3431515011 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Peripheral axonal neuropathy | true | Inferred relationship | Existential restriction modifier | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Congenital facial nerve palsy | true | Inferred relationship | Existential restriction modifier | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Congenital hypogonadotropic hypogonadism | true | Inferred relationship | Existential restriction modifier | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 4 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Facial nerve structure | true | Inferred relationship | Existential restriction modifier | 4 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 6 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Existential restriction modifier | 6 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 7 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Structure of pars distalis of pituitary | true | Inferred relationship | Existential restriction modifier | 7 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Has interpretation | Absent | true | Inferred relationship | Existential restriction modifier | 5 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Interprets | Gross movement of body and limbs | true | Inferred relationship | Existential restriction modifier | 5 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Interprets | Movement | true | Inferred relationship | Existential restriction modifier | 3 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Axon structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Finding of gross movement of body and limbs | true | Inferred relationship | Existential restriction modifier | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Nerve palsy | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets