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109271000119105: Family history of double heterozygous familial hypercholesterolemia (situation)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3664453019 Family history of double heterozygous familial hypercholesterolaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664454013 Family history of double heterozygous familial hypercholesterolemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4021915015 Family history of double heterozygous familial hypercholesterolemia (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664453019 Family history of double heterozygous familial hypercholesterolaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664454013 Family history of double heterozygous familial hypercholesterolemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664526016 Family history of familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664527013 Family history of familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664528015 Family history of familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4021915015 Family history of double heterozygous familial hypercholesterolemia (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of double heterozygous familial hypercholesterolemia Is a Family history of hereditary disease (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of double heterozygous familial hypercholesterolemia Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of double heterozygous familial hypercholesterolemia Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of double heterozygous familial hypercholesterolemia Is a Family history of familial hypercholesterolemia (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of double heterozygous familial hypercholesterolemia Associated finding Double heterozygous familial hypercholesterolaemia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of double heterozygous familial hypercholesterolemia Finding context Known present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of double heterozygous familial hypercholesterolemia Subject relationship context Person in the family true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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