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767133009: Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder)


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


0 descendants.

Expanded Value Set


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

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