Home › Entities › congenital disorder › fibular hemimelia

fibular hemimelia

congenital absence of the fibula
Class type of: congenital disorder, hemimelia, developmental defect during embryogenesis Q1411024

Facts

6 properties
Instance of
class of disease
Subclass of
congenital disorder, hemimelia, developmental defect during embryogenesis[2][3][4]
Age of onset
congenital onset[7]
Has phenotype
gait abnormality, genu valgum, Tibial bowing, non-syndromic limb reduction defect, joint hypermobility, joint stiffness, Toe syndactyly, equinus foot deformity, Bowing of the legs, femoral agenesis/hypoplasia, Finger syndactyly, oligodactyly, Proximal femoral focal deficiency, renal hypodysplasia, craniosynostosis, congenital heart disease, thrombocytopenia, spina bifida[8][9][10][11][12][13][14][15][16][17][18][19][20][21]
Health specialty
medical genetics[6]
Prevalence
+0.00005[5]
🏷️ Also known as
en longitudinal fibular deficiency en fibular hemimelia en Fibular longitudinal meromelia en Fibular longitudinal meromelia, unilateral en Congenital longitudinal deficiency of the fibula ar انعدام النصف الشظوي للطرف de fibulärer Längsdefekt de fibulare Hemimelie es Hemimelia peronea es Hemimelia es Hemimelia fibular fr hémimélie fibulaire it Assenza congenita della fibula it Emimelia fibulare ja 腓骨欠損 pl aplazja kości strzałkowej pl Hemimelia strzałkowa ro Hemimelie fibulară ru фибулярная гемимелия zh 腓骨半肢畸形
🔖 Identifiers · 15
BabelNet ID
01428162n
DiseasesDB
33931
Exact match
www.orpha.net
Freebase ID
/m/05f6yc2
GARD rare disease ID
8659
ICD-10 ID
Q72.6
ICD-11 ID (Foundation)
915482054
ICD-11 ID (MMS)
LB9A.2
Microsoft Academic ID (discontinued)
2776551591, 2911051215
Mondo ID
MONDO_0019672
Orphanet ID
93323
PatientsLikeMe condition ID
fibular-hemimelia
Show all 15 identifiers +3
Raras disease ID
D93323
UMLS CUI
C0013589, C0265634
WikiProjectMed ID
Fibular hemimelia

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Subclass of 2
congenital disorder, hemimelia
Health specialty 1
medical genetics
Press Enter · cited answer in seconds

Summary

fibular hemimelia is a class of disease[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . 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). fibular hemimelia. Retrieved November 7, 2026, from https://4ort.xyz/entity/fibular-hemimelia
MLA “fibular hemimelia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/fibular-hemimelia.
BibTeX @misc{4ortxyz_fibular-hemimelia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fibular hemimelia}}, year = {2026}, url = {https://4ort.xyz/entity/fibular-hemimelia}, note = {Accessed: 2026-11-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): fibular hemimelia — https://4ort.xyz/entity/fibular-hemimelia (retrieved 2026-11-07)

Canonical URL: https://4ort.xyz/entity/fibular-hemimelia · 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. 19d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Prevalence → 0.00005
    Age of onset → congenital onset
    Has phenotype → gait abnormality, genu valgum, Tibial bowing +1
    Raras disease ID → D93323
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Health specialty → medical genetics
    Instance of → class of disease
    Subclass of → congenital disorder, hemimelia, developmental defect during embryogenesis
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.