PanCareSurPass Project HL7 FHIR Implementation Guide
0.1.0 - trial-use 150

This page is part of the PanCareSurPass Project HL7 FHIR Implementation Guide (v0.1.0: QA Preview) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

ValueSet: Hereditary Predispositions (ICD10)

Official URL: http://hl7.eu/fhir/ig/pcsp/ValueSet/vs-icd10-predisposition-eu-pcsp Version: 0.1.0
Active as of 2023-01-26 Computable Name: ICD10HereditaryPredisposition

Hereditary Predispositions (ICD10)

References

Logical Definition (CLD)

This value set includes codes based on the following rules:

  • Include these codes as defined in http://terminology.hl7.org/CodeSystem/data-absent-reason
    CodeDisplayDefinition
    not-applicableNot ApplicableThere is no proper value for this element (e.g. last menstrual period for a male).
  • Include these codes as defined in http://hl7.org/fhir/sid/icd-10
    CodeDisplay
    D61.0Constitutional aplastic anemia
    D82.0Wiskott-Aldrich syndrome
    D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
    E34.8Other specified endocrine disorders
    G11.3Cerebellar ataxia with defective DNA repair
    K86.1Other chronic pancreatitis
    L72.8Other follicular cysts of the skin and subcutaneous tissue
    Q78.6Multiple congenital exostoses
    Q82.1Xeroderma pigmentosum
    Q82.2Congenital cutaneous mastocytosis
    Q82.8Other specified congenital malformations of skin
    Q85.0Neurofibromatosis (nonmalignant)
    Q85.1Tuberous sclerosis
    Q85.8Other phakomatoses, not elsewhere classified
    Q87.3Congenital malformation syndromes involving early overgrowth
    Q87.8Other specified congenital malformation syndromes, not elsewhere classified

 

Expansion

This value set contains 17 concepts

Expansion based on:

CodeSystemDisplayDefinition
  not-applicablehttp://terminology.hl7.org/CodeSystem/data-absent-reasonNot Applicable

There is no proper value for this element (e.g. last menstrual period for a male).

  D61.0http://hl7.org/fhir/sid/icd-10Constitutional aplastic anemia
  D82.0http://hl7.org/fhir/sid/icd-10Wiskott-Aldrich syndrome
  D82.3http://hl7.org/fhir/sid/icd-10Immunodeficiency following hereditary defective response to Epstein-Barr virus
  E34.8http://hl7.org/fhir/sid/icd-10Other specified endocrine disorders
  G11.3http://hl7.org/fhir/sid/icd-10Cerebellar ataxia with defective DNA repair
  K86.1http://hl7.org/fhir/sid/icd-10Other chronic pancreatitis
  L72.8http://hl7.org/fhir/sid/icd-10Other follicular cysts of the skin and subcutaneous tissue
  Q78.6http://hl7.org/fhir/sid/icd-10Multiple congenital exostoses
  Q82.1http://hl7.org/fhir/sid/icd-10Xeroderma pigmentosum
  Q82.2http://hl7.org/fhir/sid/icd-10Congenital cutaneous mastocytosis
  Q82.8http://hl7.org/fhir/sid/icd-10Other specified congenital malformations of skin
  Q85.0http://hl7.org/fhir/sid/icd-10Neurofibromatosis (nonmalignant)
  Q85.1http://hl7.org/fhir/sid/icd-10Tuberous sclerosis
  Q85.8http://hl7.org/fhir/sid/icd-10Other phakomatoses, not elsewhere classified
  Q87.3http://hl7.org/fhir/sid/icd-10Congenital malformation syndromes involving early overgrowth
  Q87.8http://hl7.org/fhir/sid/icd-10Other specified congenital malformation syndromes, not elsewhere classified

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code