Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3664436014 | Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3664437017 | Double heterozygous familial hypercholesterolaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3664439019 | Double heterozygous familial hypercholesterolemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3664440017 | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3664441018 | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
5066051018 | Compound heterozygous familial hypercholesterolemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5066052013 | Compound heterozygous familial hypercholesterolaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Is a | Familial hypercholesterolemia | true | Inferred relationship | Existential restriction modifier | ||
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Is a | Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations | true | Inferred relationship | Existential restriction modifier | ||
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Due to | Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations | true | Inferred relationship | Existential restriction modifier | 2 | |
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 1 | |
Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Interprets | Serum total cholesterol measurement | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Family history of double heterozygous familial hypercholesterolemia | Associated finding | True | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets