Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5045341012 | Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5045342017 | Microcephalic primordial dwarfism, insulin resistance syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
5045343010 | A rare genetic disease with characteristics of severe pre and postnatal growth failure with short stature and microcephaly, facial dysmorphism (including a small jaw and prominent midface), severe insulin resistance, fatty liver, hypertriglyceridemia developing in childhood and primary gonadal failure. Mild global learning difficulties and acanthosis nigricans have also been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
5045344016 | A rare genetic disease with characteristics of severe pre and postnatal growth failure with short stature and microcephaly, facial dysmorphism (including a small jaw and prominent midface), severe insulin resistance, fatty liver, hypertriglyceridaemia developing in childhood and primary gonadal failure. Mild global learning difficulties and acanthosis nigricans have also been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Congenital microcephaly | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Primordial dwarfism | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Hypogonadism | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Insulin resistance | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Microcephalic primordial dwarfism, insulin resistance syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 4 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Interprets | Body height | true | Inferred relationship | Some | 2 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Interprets | Birth head circumference | true | Inferred relationship | Some | 3 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Has interpretation | Below reference range | true | Inferred relationship | Some | 3 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Finding site | Structure of head | true | Inferred relationship | Some | 1 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Associated morphology | Congenital smallness | true | Inferred relationship | Some | 1 | |
Microcephalic primordial dwarfism, insulin resistance syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set