Trait
Abnormal sacrum morphology
An abnormality of the sacral bone.
Summary
- Also called
- Abnormality of the sacrum
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
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Read the genes linked to Abnormal sacrum morphology, and the rest of your genome, with one test.
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Get my Genome Test17 genes linked to Abnormal sacrum morphology
Changes in these genes cause rare conditions in which Abnormal sacrum morphology 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 |
|---|---|---|
| FGF20fibroblast growth factor 20 | Often (30–79%) | In 1 condition |
| GFRA1GDNF family receptor alpha 1 | Often (30–79%) | In 1 condition |
| GREB1LGREB1 like retinoic acid receptor coactivator | Often (30–79%) | In 1 condition |
| ITGA8integrin subunit alpha 8 | Often (30–79%) | In 1 condition |
| RETret proto-oncogene | Often (30–79%) | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Often (30–79%) | In 1 condition |
| WNT9BWnt family member 9B | Often (30–79%) | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Sometimes (5–29%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Sometimes (5–29%) | In 1 condition |
| GDF3growth differentiation factor 3 | Sometimes (5–29%) | In 1 condition |
| GDF6growth differentiation factor 6 | Sometimes (5–29%) | In 1 condition |
| HOXD13homeobox D13 | Sometimes (5–29%) | In 1 condition |
| MEOX1mesenchyme homeobox 1 | Sometimes (5–29%) | In 1 condition |
| NOTCH3notch receptor 3 | Sometimes (5–29%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| SRD5A3steroid 5 alpha-reductase 3 | Sometimes (5–29%) | In 1 condition |
| TBX6T-box transcription factor 6 | Sometimes (5–29%) | 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.
Narrower traits
- Abnormal sacroiliac joint morphology5 genes
- Absent/small sacrum4 genes
- Sacrococcygeal teratoma4 genes
- Horizontal sacrum3 genes
- Absence of some of the sacral and coccygeal bones2 genes
- Sacrococcygeal pilonidal abnormality1 gene
- Abnormal ossification of the sacrum
- Sacral meningocele
- Sacral segmentation defect
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 2026.10.16-c6eea6bf.
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