Trait
Subarachnoid hemorrhage
Hemorrhage occurring between the arachnoid mater and the pia mater.
Reference genomeGRCh38hg38
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Get my Genome Test41 genes linked to Subarachnoid hemorrhage
Changes in these genes cause rare conditions in which Subarachnoid hemorrhage 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 |
|---|---|---|
| GAAalpha glucosidase | Always | In 1 condition |
| THSD1thrombospondin type 1 domain containing 1 | Often (30–79%) | In 2 conditions |
| ACTA2actin alpha 2, smooth muscle | Sometimes (5–29%) | In 1 condition |
| ACVRL1activin A receptor like type 1 | Sometimes (5–29%) | In 2 conditions |
| ANGPTL6angiopoietin like 6 | Sometimes (5–29%) | In 1 condition |
| APPamyloid beta precursor protein | Sometimes (5–29%) | In 1 condition |
| COL3A1collagen type III alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Sometimes (5–29%) | In 1 condition |
| ELNelastin | Sometimes (5–29%) | In 1 condition |
| ENGendoglin | Sometimes (5–29%) | In 3 conditions |
| FBN1fibrillin 1 | Sometimes (5–29%) | In 1 condition |
| FOXE3forkhead box E3 | Sometimes (5–29%) | In 1 condition |
| GDF2growth differentiation factor 2 | Sometimes (5–29%) | In 1 condition |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Sometimes (5–29%) | In 1 condition |
| LOXlysyl oxidase | Sometimes (5–29%) | In 1 condition |
| MAT2Amethionine adenosyltransferase 2A | Sometimes (5–29%) | In 1 condition |
| MFAP5microfibril associated protein 5 | Sometimes (5–29%) | In 1 condition |
| MYH11myosin heavy chain 11 | Sometimes (5–29%) | In 1 condition |
| MYLKmyosin light chain kinase | Sometimes (5–29%) | In 1 condition |
| PRKG1protein kinase cGMP-dependent 1 | Sometimes (5–29%) | In 1 condition |
| RASA1RAS p21 protein activator 1 | Sometimes (5–29%) | In 1 condition |
| SMAD2SMAD family member 2 | Sometimes (5–29%) | In 1 condition |
| SMAD3SMAD family member 3 | Sometimes (5–29%) | In 2 conditions |
| SMAD4SMAD family member 4 | Sometimes (5–29%) | In 2 conditions |
| STIM1stromal interaction molecule 1 | Sometimes (5–29%) | In 1 condition |
| TGFB2transforming growth factor beta 2 | Sometimes (5–29%) | In 1 condition |
| TGFB3transforming growth factor beta 3 | Sometimes (5–29%) | In 1 condition |
| TGFBR1transforming growth factor beta receptor 1 | Sometimes (5–29%) | In 1 condition |
| TGFBR2transforming growth factor beta receptor 2 | Sometimes (5–29%) | In 1 condition |
| TGFBR3transforming growth factor beta receptor 3 | Sometimes (5–29%) | In 1 condition |
| THSD4thrombospondin type 1 domain containing 4 | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| ADA2adenosine deaminase 2 | Rarely (1–4%) | In 1 condition |
| CD109CD109 molecule | Rarely (1–4%) | In 1 condition |
| F10coagulation factor X | Rarely (1–4%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Rarely (1–4%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Rarely (1–4%) | In 1 condition |
| ITGA2integrin subunit alpha 2 | Rarely (1–4%) | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Rarely (1–4%) | In 1 condition |
| ITGB3integrin subunit beta 3 | Rarely (1–4%) | In 1 condition |
Show 1 more gene
| Gene | How often it is seen | Conditions |
|---|---|---|
| DOCK8dedicator of cytokinesis 8 | 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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