This page is part of the Genetic Reporting Implementation Guide (v2.0.0: STU 2) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Summary
Defining URL: | http://hl7.org/fhir/uv/genomics-reporting/ValueSet/condition-inheritance-mode-vs |
Version: | 2.0.0 |
Name: | ConditionInheritanceModeVS |
Title: | Condition Inheritance Patterns |
Status: | Active as of 2022-05-09 04:59:16+0000 |
Definition: | Value Set for specific transmission patterns of a condition in a pedigree |
Publisher: | HL7 Clinical Genomics Working Group |
Source Resource: | XML / JSON / Turtle |
References
This value set includes codes based on the following rules:
http://www.ebi.ac.uk/ols/ontologies/geno
Code | Display |
0000143 | Codominant inheritance |
0000889 | Unknown inheritance |
0000892 | Mitochondrial inheritance (primarily or exclusively heteroplasmic) |
0000893 | Mitochondrial inheritance (primarily or exclusively homoplasmic) |
http://hpo.jax.org/app/
Code | Display |
0000006 | Autosomal dominant inheritance |
0000007 | Autosomal recessive inheritance |
0001417 | X-linked inheritance |
0001419 | X-linked inheritance (recessive) |
0001423 | X-linked inheritance (dominant) |
0001426 | Multifactorial inheritance |
0001427 | Mitochondrial inheritance |
0001428 | Somatic mutation |
0001450 | Y-linked inheritance |
0001470 | Autosomal dominant inheritance (sex-limited) |
0003743 | Genetic anticipation |
0003745 | Sporadic |
0010983 | Oligogenic |
0012274 | Autosomal dominant inheritance (with paternal imprinting) |
0012275 | Autosomal dominant inheritance (with maternal imprinting) |
0025352 | Autosomal dominant inheritance (primarily or exclusively de novo) |
0031362 | Autosomal recessive inheritance (sex-limited) |
http://purl.obolibrary.org/obo/sepio-clingen
Code | Display |
97020 | Semidominant inheritance |
97021 | X-linked inheritance (primarily recessive with milder female expression) |
97022 | Autosomal dominant inheritance (with genetic anticipation) |
97023 | Autosomal recessive inheritance (with genetic anticipation) |
No Expansion for this valueset (Unknown Code System)
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 |
Source | 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 |