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lethal encephalopathy due to mitochondrial and peroxisomal fission defect

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784313
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lethal encephalopathy due to mitochondrial and peroxisomal fission defect

Summary

lethal encephalopathy due to mitochondrial and peroxisomal fission defect is a developmental defect during embryogenesis[1].

Key Facts

  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's instance of is recorded as developmental defect during embryogenesis[2].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's instance of is recorded as rare disease[3].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's instance of is recorded as class of disease[4].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect is a type of mitochondrial oxidative phosphorylation disorder with no known mechanism[5].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect is a type of rare genetic developmental defect during embryogenesis[6].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect is a type of neurometabolic disease[7].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's genetic association is recorded as DNM1L[8].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's genetic association is recorded as MFF[9].
  • lethal encephalopathy due to mitochondrial and peroxisomal fission defect's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_330050[10].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  8. [9] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [10] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). lethal encephalopathy due to mitochondrial and peroxisomal fission defect. Retrieved May 3, 2026, from https://4ort.xyz/entity/lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect
MLA “lethal encephalopathy due to mitochondrial and peroxisomal fission defect.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect.
BibTeX @misc{4ortxyz_lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lethal encephalopathy due to mitochondrial and peroxisomal fission defect}}, year = {2026}, url = {https://4ort.xyz/entity/lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lethal encephalopathy due to mitochondrial and peroxisomal fission defect — https://4ort.xyz/entity/lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/lethal-encephalopathy-due-to-mitochondrial-and-peroxisomal-fission-defect · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 4d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0054865
    Genetic association → DNM1L, MFF
    Kegg id → H01900
    Orphanet id → 330050
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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