Trait
Low glucose levels in cerebral spinal fluid
Clinical name: Hypoglycorrhachia
Abnormally low glucose concentration in the cerebrospinal fluid.
Summary
- Also called
- Decreased CSF glucose
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Low glucose levels in cerebral spinal fluid
Changes in these genes cause rare conditions in which Low glucose levels in cerebral spinal fluid 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 |
|---|---|---|
| SLC2A1solute carrier family 2 member 1 | Always | In 5 conditions |
| TBK1TANK binding kinase 1 | Sometimes (5–29%) | In 1 condition |
| TICAM1TIR domain containing adaptor molecule 1 | Sometimes (5–29%) | In 1 condition |
| TLR3toll like receptor 3 | Sometimes (5–29%) | In 1 condition |
| TRAF3TNF receptor associated factor 3 | Sometimes (5–29%) | In 1 condition |
| UNC93B1unc-93B1 regulator of TLR signaling | 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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