Trait
Abnormal cochlea morphology
An abnormality of the cochlea.
Summary
- Also called
- Abnormality of cochlea
- Body system
- Abnormality of the ear
Reference genomeGRCh38hg38
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Read the genes linked to Abnormal cochlea morphology, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Abnormal cochlea morphology
Changes in these genes cause rare conditions in which Abnormal cochlea 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 |
|---|---|---|
| ARSGarylsulfatase G | Very often (80–99%) | In 1 condition |
| CDH23cadherin related 23 | Very often (80–99%) | In 1 condition |
| CEP78centrosomal protein 78 | Very often (80–99%) | In 1 condition |
| CLRN1clarin 1 | Very often (80–99%) | In 1 condition |
| ESPNespin | Very often (80–99%) | In 1 condition |
| HARS1histidyl-tRNA synthetase 1 | Very often (80–99%) | In 1 condition |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Very often (80–99%) | In 1 condition |
| MYO7Amyosin VIIA | Very often (80–99%) | In 1 condition |
| PCDH15protocadherin related 15 | Very often (80–99%) | In 1 condition |
| USH1CUSH1 protein network component harmonin | Very often (80–99%) | In 1 condition |
| USH1GUSH1 protein network component sans | Very often (80–99%) | In 1 condition |
| NDPnorrin cystine knot growth factor NDP | Often (30–79%) | In 1 condition |
| POU3F4POU class 3 homeobox 4 | Often (30–79%) | In 1 condition |
| TIMM8Atranslocase of inner mitochondrial membrane 8A | Often (30–79%) | In 1 condition |
| SETBP1SET binding protein 1 | 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.
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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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