SNOMED_CT

SNOMED CT Concept 1388630003: SLC25A42 gene-related mitochondrial encephalomyopathy

1388630003 is a SNOMED CT concept used to represent SLC25A42 gene-related mitochondrial encephalomyopathy in structured clinical data. You may see this concept in clinical documentation systems, problem lists, terminology services, interoperability records, or semantic mapping workflows. SNOMED CT is a clinical terminology used to capture healthcare meaning in a standardized, interoperable form. This concept is typed as a disorder in the terminology hierarchy.

Reviewed by HealthAssure Clinical TeamUpdated 26 May 2026

What is this code?

SNOMED CT is a clinical terminology used to capture healthcare meaning in a standardized, interoperable form. This concept is typed as a disorder in the terminology hierarchy.

When is it used?

  • Used to represent a standardized clinical concept in health records, terminology services, and semantic mappings.
  • Often linked to diagnoses, findings, procedures, body structures, organisms, substances, or observable entities depending on the concept type.
  • Semantic tag: disorder

What it does not mean

  • A terminology concept label alone does not replace clinical interpretation, diagnosis context, or treatment advice.

Key facts

Semantic tagDisorder
Definition statusPrimitive
Definition patternSubclass
OWL axioms1
Defining attributes2
Role groups2
Module900000000000207008
Parents4

Defining attributes

Finding siteBrain structure(body structure)
Finding siteSkeletal muscle structure(body structure)

Where you may see this code

You may see this concept in clinical documentation systems, problem lists, terminology services, interoperability records, or semantic mapping workflows.

Common synonyms

Solute carrier family 25, member 42 gene-related mitochondrial encephalomyopathySLC25A42-related mitochondrial coenzyme A transporter deficiency

Frequently asked questions

Code details

Code1388630003
SystemSNOMED_CT
Display nameSLC25A42 gene-related mitochondrial encephalomyopathy
DescriptionSolute carrier family 25, member 42 gene-related mitochondrial encephalomyopathy (disorder)

Flags

BillableNo
Valid clinical useNo

Source

SourceSNOMED CT
Version20260501T120000Z
Releasesnapshot

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from SNOMED CT. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.

SNOMED CT 1388630003 | SLC25A42 gene-related mitochondrial encephalomyopathy | HealthAssure