Distal hereditary motor neuropathy type V

human disease
MedicalCondition rare_disease Q28134983
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Summary

Distal hereditary motor neuropathy type V is a rare disease[1]. It draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]

Key Facts

  • Distal hereditary motor neuropathy type V's instance of is recorded as rare disease[3].
  • Distal hereditary motor neuropathy type V's instance of is recorded as class of disease[4].
  • Distal hereditary motor neuropathy type V's subclass of is recorded as Distal hereditary motor neuropathies[5].
  • Distal hereditary motor neuropathy type V's OMIM ID is recorded as 600794[6].
  • Distal hereditary motor neuropathy type V's OMIM ID is recorded as 614751[7].
  • Distal hereditary motor neuropathy type V's Orphanet ID is recorded as 139536[8].
  • Distal hereditary motor neuropathy type V's genetic association is recorded as REEP1[9].
  • Distal hereditary motor neuropathy type V's genetic association is recorded as GARS1[10].
  • Distal hereditary motor neuropathy type V's genetic association is recorded as BSCL2[11].
  • Distal hereditary motor neuropathy type V's UMLS CUI is recorded as C1833308[12].
  • Distal hereditary motor neuropathy type V's ICD-10-CM is recorded as G12.2[13].
  • Distal hereditary motor neuropathy type V's Mondo ID is recorded as MONDO_0015353[14].
  • Distal hereditary motor neuropathy type V's Microsoft Academic ID is recorded as 2911041754[15].
  • Distal hereditary motor neuropathy type V's WikiProjectMed ID is recorded as Distal hereditary motor neuropathy type V[16].

Why It Matters

Distal hereditary motor neuropathy type V draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V.. wikidata.org.
  8. [10] ↑ . Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [11] ↑ . Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome. wikidata.org.
  10. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). Distal hereditary motor neuropathy type V. Retrieved October 16, 2026, from https://4ort.xyz/entity/distal-hereditary-motor-neuropathy-type-v
MLA “Distal hereditary motor neuropathy type V.” 4ort.xyz Knowledge Graph, 4ort.xyz, 16 Oct. 2026, https://4ort.xyz/entity/distal-hereditary-motor-neuropathy-type-v.
BibTeX @misc{4ortxyz_distal-hereditary-motor-neuropathy-type-v_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Distal hereditary motor neuropathy type V}}, year = {2026}, url = {https://4ort.xyz/entity/distal-hereditary-motor-neuropathy-type-v}, note = {Accessed: 2026-10-16}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Distal hereditary motor neuropathy type V — https://4ort.xyz/entity/distal-hereditary-motor-neuropathy-type-v (retrieved 2026-10-16)

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