Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Traits
Traits linked to GLDN
gliomedin
The Human Phenotype Ontology links 33 traits to GLDN, by body system: features seen in people with one of the gene's rare conditions.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Little lower jaw | Very often (80–99%) |
| Cleft palate | Often (30–79%) |
| Cystic hygroma | Often (30–79%) |
| Depressed nasal bridge | Often (30–79%) |
| Dandy-Walker malformation | Sometimes (5–29%) |
| Receding chin | Sometimes (5–29%) |
| Small retruded chin | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Arthrogryposis multiplex congenita | Very often (80–99%) |
| Multiple joint contractures | Very often (80–99%) |
| Diffuse skeletal muscle wasting | Often (30–79%) |
| Scoliosis | Often (30–79%) |
| Distal arthrogryposis | Sometimes (5–29%) |
| Flexed joint that cannot be straightened | Sometimes (5–29%) |
| Permanent flexion of the finger or toe | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Absent palm lines | Very often (80–99%) |
| Permanent flexion of the finger | Very often (80–99%) |
| Flexion contracture of finger | Often (30–79%) |
| Club foot on both sides | Sometimes (5–29%) |
| Elbow flexion contracture | Sometimes (5–29%) |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| High levels of amniotic fluid | Always |
| Less than 10 fetal movements in 12 hours | Always |
| Fetal akinesia sequence | Very often (80–99%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Akinesia | Very often (80–99%) |
| Decreased muscle movement | Very often (80–99%) |
| Excessive daytime sleepiness | Very often (80–99%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Poorly developed lungs | Very often (80–99%) |
| Respiratory function loss | Very often (80–99%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Underdeveloped instestine | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Ears rotated toward back of head | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Often (30–79%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Undescended testes | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Pterygium | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Prenatal growth deficiency | Very often (80–99%) |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to GLDN and how often each is seen. Find out more at hpo.jax.org.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks