PanCareSurPass Project HL7 FHIR Implementation Guide
1.0.0 - release 150

PanCareSurPass Project HL7 FHIR Implementation Guide, published by PanCareSurPass Project. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/pcsp/ and changes regularly. 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: 1.0.0
Active as of 2025-10-16 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 version 📦1.0.0
    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 version Not Stated (use latest from terminology server)
    CodeDisplay
    D61.0 Constitutional aplastic anemia
    D82.0 Wiskott-Aldrich syndrome
    D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
    E34.8 Other specified endocrine disorders
    G11.3 Cerebellar ataxia with defective DNA repair
    K86.1 Other chronic pancreatitis
    L72.8 Other follicular cysts of the skin and subcutaneous tissue
    Q78.6 Multiple congenital exostoses
    Q82.1 Xeroderma pigmentosum
    Q82.2 Congenital cutaneous mastocytosis
    Q82.8 Other specified congenital malformations of skin
    Q85.0 Neurofibromatosis (nonmalignant)
    Q85.1 Tuberous sclerosis
    Q85.8 Other phakomatoses, not elsewhere classified
    Q87.3 Congenital malformation syndromes involving early overgrowth
    Q87.8 Other specified congenital malformation syndromes, not elsewhere classified

 

Expansion

Expansion from tx.fhir.org based on:

This value set contains 17 concepts

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