Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test21 genes linked to Hoarse cry
Changes in these genes cause rare conditions in which Hoarse cry 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 |
|---|---|---|
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Always | In 1 condition |
| KRT14keratin 14 | Always | In 1 condition |
| KRT5keratin 5 | Always | In 1 condition |
| LAMA3laminin subunit alpha 3 | Always | In 2 conditions |
| NSD1nuclear receptor binding SET domain protein 1 | Always | In 1 condition |
| ASAH1N-acylsphingosine amidohydrolase 1 | Often (30–79%) | In 2 conditions |
| FOXE1forkhead box E1 | Often (30–79%) | In 1 condition |
| NKX2-1NK2 homeobox 1 | Often (30–79%) | In 1 condition |
| NKX2-5NK2 homeobox 5 | Often (30–79%) | In 1 condition |
| PAX8paired box 8 | Often (30–79%) | In 2 conditions |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Often (30–79%) | In 1 condition |
| SLC26A4solute carrier family 26 member 4 | Often (30–79%) | In 1 condition |
| TSHBthyroid stimulating hormone subunit beta | Often (30–79%) | In 2 conditions |
| TSHRthyroid stimulating hormone receptor | Often (30–79%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| DUOX2dual oxidase 2 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| LTBP4latent transforming growth factor beta binding protein 4 | Sometimes (5–29%) | In 1 condition |
| MEG3maternally expressed 3 | Sometimes (5–29%) | In 1 condition |
| RTL1retrotransposon Gag like 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.
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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