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Trait
Hypoplastic iliac wing
Underdevelopment of the ilium ala.
Summary
- Also called
- Hypoplastic iliac alae, Hypoplastic iliac wings, Small iliac wings
- Body system
- Abnormality of the musculoskeletal system
Hypoplastic iliac wingHP:0002866
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Read the genes linked to Hypoplastic iliac wing, and the rest of your genome, with one test.
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Get my Genome Test31 genes linked to Hypoplastic iliac wing
Changes in these genes cause rare conditions in which Hypoplastic iliac wing 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 |
|---|---|---|
| BNIP1BCL2 interacting protein 1 | Always | In 1 condition |
| NKX3-2NK3 homeobox 2 | Always | In 1 condition |
| SMAD4SMAD family member 4 | Always | In 1 condition |
| TBX15T-box transcription factor 15 | Always | In 1 condition |
| HDAC6histone deacetylase 6 | Very often (80–99%) | In 2 conditions |
| PCNTpericentrin | Very often (80–99%) | In 2 conditions |
| COL9A1collagen type IX alpha 1 chain | Often (30–79%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Often (30–79%) | In 1 condition |
| DYMdymeclin | Often (30–79%) | In 1 condition |
| LAMA5laminin subunit alpha 5 | Often (30–79%) | In 1 condition |
| MEG3maternally expressed 3 | Often (30–79%) | In 1 condition |
| RIPK4receptor interacting serine/threonine kinase 4 | Often (30–79%) | In 1 condition |
| RTL1retrotransposon Gag like 1 | Often (30–79%) | In 1 condition |
| WNT7AWnt family member 7A | Often (30–79%) | In 1 condition |
| CTSKcathepsin K | Sometimes (5–29%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Rarely (1–4%) | In 2 conditions |
| FN1fibronectin 1 | Rarely (1–4%) | In 1 condition |
| ARSBarylsulfatase B | Not recorded | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Not recorded | In 1 condition |
| CREBBPCREB binding lysine acetyltransferase | Not recorded | In 1 condition |
| EEDembryonic ectoderm development | Not recorded | In 1 condition |
| EP300EP300 lysine acetyltransferase | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Not recorded | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Not recorded | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Not recorded | In 1 condition |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Not recorded | In 1 condition |
| IHHIndian hedgehog signaling molecule | Not recorded | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Not recorded | In 1 condition |
| SOX9SRY-box transcription factor 9 | Not recorded | In 1 condition |
| TRAPPC2trafficking protein particle complex subunit 2 | 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 2026.10.16-c6eea6bf.
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