sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome

human disease

MedicalCondition developmental_defect_during_embryogenesis Q55784776

Press Enter · cited answer in seconds

sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome

Summary

sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome is a developmental defect during embryogenesis^[1].

Key Facts

sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome's instance of is recorded as rare disease^[3].
sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome's instance of is recorded as class of disease^[4].
sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome is a type of malformation of the neurenteric canal, spinal cord and column^[5].
sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome's genetic association is recorded as TBXT^[6].
sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_397927^[7].

⭐ Popularity Graph

0/100 long tail

Quick Facts

Instance of rare disease, class of disease

Subclass of malformation of the neurenteric canal, spinal cord and column, developmental defect during embryogenesis

Properties

Exact match www.orpha.net

Genetic association TBXT

External References (7)

Icd-10-cm Q87.5

Kegg id H02324

Mondo id MONDO_0014314

Omim id 615709

Orphanet id 397927

Umls cui C3810343, C4751569

Uniprot disease id DI-04072

References

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

Direct Wikidata claims

[2] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — instance of (P31): rare disease. wikidata.org.
[4] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — instance of (P31): class of disease. wikidata.org.
[5] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — subclass of (P279): malformation of the neurenteric canal, spinal cord and column. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[6] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — genetic association (P2293): TBXT. Q905695. Retrieved 2019-08-13. wikidata.org.
[7] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_397927. wikidata.org.

Class ancestry

[1] ↑ sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome is an instance of developmental defect during embryogenesis (Q55788864) [P31, primary]. 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). sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome

MLA

“sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome.

BibTeX

@misc{4ortxyz_sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome — https://4ort.xyz/entity/sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/sacral-agenesis-abnormal-ossification-of-the-vertebral-bodies-persistent-notochordal-canal-syndrome · Last refreshed: May 3, 2026

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.

5w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0014314

Genetic association → TBXT

Kegg id → H02324

Orphanet id → 397927

+ 9 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"

Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.