Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3431514010 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3431515011 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3431516012 | A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Interprets | Movement | true | Inferred relationship | Some | 3 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Axon structure | true | Inferred relationship | Some | 1 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Gross movement of body and limbs - finding | true | Inferred relationship | Some | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Nerve palsy | true | Inferred relationship | Some | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Peripheral axonal neuropathy | true | Inferred relationship | Some | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Congenital facial nerve palsy | true | Inferred relationship | Some | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Is a | Congenital hypogonadotropic hypogonadism | true | Inferred relationship | Some | ||
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Facial nerve structure | true | Inferred relationship | Some | 4 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 6 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 6 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 7 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Finding site | Structure of distal part of pituitary | true | Inferred relationship | Some | 7 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Has interpretation | Absent | true | Inferred relationship | Some | 5 | |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | Interprets | Gross movement of body and limbs | true | Inferred relationship | Some | 5 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Queensland allied health indicator for intervention reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set