Trait
Absent calf bone
Clinical name: Fibular aplasia
Absence of the fibula.
Summary
- Also called
- Absent fibulae, Absent-hypoplastic fibulae
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/fibular-aplasia.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Absent calf bone, and the rest of your genome, with one test.
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Get my Genome Test10 genes linked to Absent calf bone
Changes in these genes cause rare conditions in which Absent calf bone is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| BMPR1Bbone morphogenetic protein receptor type 1B | Always | In 1 condition |
| FLNBfilamin B | Always | In 3 conditions |
| GDF5growth differentiation factor 5 | Very often (80–99%) | In 1 condition |
| LMBR1limb development membrane protein 1 | Very often (80–99%) | In 2 conditions |
| WNT7AWnt family member 7A | Very often (80–99%) | In 3 conditions |
| FLNAfilamin A | Often (30–79%) | In 1 condition |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| RBM8ARNA binding motif protein 8A | Sometimes (5–29%) | In 2 conditions |
| AMER1APC membrane recruitment protein 1 | Not recorded | In 1 condition |
| TBX15T-box transcription factor 15 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
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