Athabaskan brainstem dysgenesis syndrome

Human disease
MedicalCondition rare_disease Q18553396
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Athabaskan brainstem dysgenesis syndrome

Summary

Athabaskan brainstem dysgenesis syndrome is a rare disease[1]. It draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]

Key Facts

  • Athabaskan brainstem dysgenesis syndrome's instance of is recorded as rare disease[3].
  • Athabaskan brainstem dysgenesis syndrome's instance of is recorded as class of disease[4].
  • Athabaskan brainstem dysgenesis syndrome's subclass of is recorded as autosomal recessive disease[5].
  • Athabaskan brainstem dysgenesis syndrome's subclass of is recorded as encephalopathy[6].
  • Athabaskan brainstem dysgenesis syndrome's OMIM ID is recorded as 601536[7].
  • Athabaskan brainstem dysgenesis syndrome's Disease Ontology ID is recorded as DOID:0050682[8].
  • Athabaskan brainstem dysgenesis syndrome's Orphanet ID is recorded as 69739[9].
  • Athabaskan brainstem dysgenesis syndrome's MalaCards ID is recorded as athabaskan_brainstem_dysgenesis_syndrome[10].
  • Athabaskan brainstem dysgenesis syndrome's genetic association is recorded as HOXA1[11].
  • Athabaskan brainstem dysgenesis syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050682[12].
  • Athabaskan brainstem dysgenesis syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050682[13].
  • Athabaskan brainstem dysgenesis syndrome's UMLS CUI is recorded as C1832215[14].
  • Athabaskan brainstem dysgenesis syndrome's GARD rare disease ID is recorded as 8333[15].
  • Athabaskan brainstem dysgenesis syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
  • Athabaskan brainstem dysgenesis syndrome's UniProt disease ID is recorded as DI-01193[17].

Why It Matters

Athabaskan brainstem dysgenesis syndrome 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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  12. [14] . UMLS 2023. Retrieved . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . 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). Athabaskan brainstem dysgenesis syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/athabaskan-brainstem-dysgenesis-syndrome
MLA “Athabaskan brainstem dysgenesis syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/athabaskan-brainstem-dysgenesis-syndrome.
BibTeX @misc{4ortxyz_athabaskan-brainstem-dysgenesis-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Athabaskan brainstem dysgenesis syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/athabaskan-brainstem-dysgenesis-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Athabaskan brainstem dysgenesis syndrome — https://4ort.xyz/entity/athabaskan-brainstem-dysgenesis-syndrome (retrieved 2026-05-03)

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