74042-3
Genetic diseases history panel Family member HL7.VMR-CDS
Active
74023-3 Disease of interest in family member
Term Description
This observation is used to report a disease of interest (e.g. malignant tumor of the breast) in the patient's family. The disease may or may not be present in a family member. The term is paired with a negation indicator [LOINC: 74022-5] to indicate whether the health history for a given family member is negative for the disease. Although similar in nature to LOINC 54116-9 (History of diseases in family member), this code does not indicate a disease in a family member. This term was created for, but not limited in use to, the clinical observation in the Family History section of the V2 VMR based on the Family History Standard Implementation Guide (US Realm) 2012. The recommended code system for answer values is SNOMED CT.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Disease of interest
- Property
- Find
- Time
- Pt
- System
- ^Family member
- Scale
- Nom
- Method
Additional Names
- Panel Name
- Short Name
- Disease of interest Fam Mem
Basic Attributes
- Class
- H&P.HX
- Type
- Clinical
- First Released
- Version 2.46
- Last Updated
- Version 2.46
- Order vs. Observation
- Observation
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 74028-2 | Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-MX | Spanish (Mexico) | Enfermedad de interés: |
| it-IT | Italian (Italy) | Malattia di interesse: Synonyms: Anamnesi Osservazione Punto nel tempo (episodio) |
| ru-RU | Russian (Russian Federation) | Искомая болезнь: Synonyms: Номинальный; |
| zh-CN | Chinese (China) | 所感兴趣疾病: Synonyms: 分类型应答; |
74022-5 Negative history for disease of interest in family member
Term Description
Used to report if the disease of interest is not present in a family member. This term was created for, but not limited in use to, the negation indicator used in the Family History section of the V2 VMR, based on the Family History Standard Implementation Guide (US Realm) 2012. Expected results are true or false, where true indicates there is no history of a given disease of interest.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Negative history for disease of interest
- Property
- Find
- Time
- Pt
- System
- ^Family member
- Scale
- Ord
- Method
Additional Names
- Panel Name
- Short Name
- Neg hx for disease Fam Mem
Basic Attributes
- Class
- H&P.HX
- Type
- Clinical
- First Released
- Version 2.46
- Last Updated
- Version 2.46
- Order vs. Observation
- Observation
Example Answer List LL1182-6
| Answer | Code | Score | Answer ID |
|---|---|---|---|
| True | 1 | LA14495-8 | |
| False | 2 | LA14496-6 |
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 74028-2 | Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-MX | Spanish (Mexico) | Historia negativa de la enfermedad de interés: |
| it-IT | Italian (Italy) | Anamnesi negativa per la malattia di interesse: Synonyms: Anamnesi Osservazione Punto nel tempo (episodio) |
| ru-RU | Russian (Russian Federation) | Отрицательная история искомой болезни: Synonyms: Порядковый Точка во времени; |
| zh-CN | Chinese (China) | 所感兴趣疾病阴性史: Synonyms: Neg 不存在的 依次型; |
74044-9 Disease of interest was cause of death in family member
Term Description
Indicates whether the family member's death was caused by the disease of interest (e.g. malignant tumor of the breast) [LOINC: 74023-3].
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Disease of interest was cause of death
- Property
- Find
- Time
- Pt
- System
- ^Family member
- Scale
- Ord
- Method
Additional Names
- Panel Name
- Short Name
- Disease was COD Fam Mem
Basic Attributes
- Class
- H&P.HX
- Type
- Clinical
- First Released
- Version 2.46
- Last Updated
- Version 2.70
- Change Reason
- Release 2.70: ANSWER_LIST_TYPE: Removed the NORMATIVE answer list type binding to the instance of the VMR-CDS panel. ; METHOD_TYP: Removed method since this concept is not specific for HL7.VMR-CDS.;
- Order vs. Observation
- Both
Normative Answer List LL1182-6
| Answer | Code | Score | Answer ID |
|---|---|---|---|
| True | 1 | LA14495-8 | |
| False | 2 | LA14496-6 |
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 74028-2 | Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-MX | Spanish (Mexico) | Enfermedad de interés fue causa de muerte: |
| it-IT | Italian (Italy) | Malattia di interesse è stato causa di morte: Synonyms: Anamnesi Osservazione Punto nel tempo (episodio) |
| ru-RU | Russian (Russian Federation) | Искомая болезнь была причиной смерти: Synonyms: Порядковый Точка во времени; |
| zh-CN | Chinese (China) | 所感兴趣疾病为死亡原因: Synonyms: 依次型; |
21611-9 Age estimated
Term Description
For situations where birthdate is unknown; age is estimated by third party on basis of physical evidence
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Age
- Property
- Time
- Time
- Pt
- System
- ^Patient
- Scale
- Qn
- Method
- Estimated
Additional Names
- Panel Name
- Short Name
- Age Time Patient Est
- Display Name
- Age Est
- Consumer Name Alpha Get Info
- Age
Basic Attributes
- Class
- MISC
- Type
- Laboratory
- First Released
- Version 1.0m
- Last Updated
- Version 2.71
- Order vs. Observation
- Observation
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 74028-2 | Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-AR | Spanish (Argentina) | edad: |
| es-ES | Spanish (Spain) | Edad: Synonyms: Cuantitativo |
| es-MX | Spanish (Mexico) | Edad: |
| et-EE | Estonian (Estonia) | Vanus: Synonyms: Juhuslik Kvantitatiivne |
| fr-BE | French (Belgium) | Âge: |
| fr-CA | French (Canada) | Âge: |
| fr-FR | French (France) | Âge: |
| it-IT | Italian (Italy) | Età: Synonyms: Miscellanea paziente Punto nel tempo (episodio) Tempo (e.g. secondi) |
| nl-NL | Dutch (Netherlands) | leeftijd: |
| pt-BR | Portuguese (Brazil) | Idade: Synonyms: Point in time; |
| tr-TR | Turkish (Turkey) | Yaş: |
| zh-CN | Chinese (China) | 年龄: Synonyms: 医疗服务对象; |
Example Units
| Unit | Source |
|---|---|
| a | Example UCUM Units |
48018-6 Gene studied [ID]
Term Description
HUGO Gene Nomenclature Committee (HGNC) identifier for a gene. List the gene(s) examined in full or in part by the study. If the study addresses multiple genes, these can be recorded in one OBX as a list seperated by repeat delimiters or in mulltiple OBX's with one gene per OBX. The recommended coding system will use the HGNC gene symbol as the display text and HGNC gene ID as the code. For example, 21497^ACAD9^HGNC.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Gene identifier
- Property
- ID
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Nom
- Method
Additional Names
- Panel Name
- Short Name
- Gene studied ID
- Display Name
- Gene studied Nom (Bld/Tiss) [ID]
- Consumer Name Alpha Get Info
- Gene studied, Blood or tissue specimen
Basic Attributes
- Class
- HL7.GENETICS
- Type
- Laboratory
- First Released
- Version 2.21
- Last Updated
- Version 2.73
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 9796
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 77313-5 | DNA analysis discrete sequence variation basic associated observations panel - Blood or Tissue by Molecular genetics method |
| 53042-8 | DNA marker assessed panel |
| 53044-4 | DNA marker identified panel |
| 51960-3 | DNA marker results panel |
| 55233-1 | Genetic analysis master panel |
| 48015-2 | Individual allele panel |
| 51975-1 | Individual allele results panel |
| 81247-9 | Master HL7 genetic variant reporting panel |
| 78046-0 | Pharmacogenomic analysis basic associated observations panel - Blood or Tissue |
| 102118-7 | Rhabdomyolysis and Metabolic myopathy multigene panel - Blood or Tissue by Molecular genetics method |
| 48014-5 | Sequence variation panel - Blood or Tissue by Molecular genetics method |
| 48017-8 | Sequencing methodology panel - Blood or Tissue by Molecular genetics method |
| 102119-5 | Skeletal muscle channelopathy multigene panel - Blood or Tissue by Molecular genetics method |
| 74028-2 | Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-MX | Spanish (Mexico) | Identificador de gen estudiado: |
| es-ES | Spanish (Spain) | Identificador genético: |
| fr-FR | French (France) | Gène identifiant: |
| it-IT | Italian (Italy) | Gene, identificatore: Synonyms: Identificatore Identificatore del gene Punto nel tempo (episodio) Referto clinico di test genetico Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | gen-identificator: |
| pt-BR | Portuguese (Brazil) | Identificação do gene: Synonyms: ; |
| ru-RU | Russian (Russian Federation) | Ген идентификатор: Synonyms: Идентификатор Кровь Кровь или Ткань Номинальный; |
| tr-TR | Turkish (Turkey) | Gen tanımlayıcı: |
| zh-CN | Chinese (China) | 基因标识符: Synonyms: HL7 遗传学 全血或组织; |