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Traits
Traits linked to LPIN1
lipin 1
The Human Phenotype Ontology links 38 traits to LPIN1, by body system: features seen in people with one of the gene's rare conditions.
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Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Elevated blood creatine phosphokinase | Always |
| Increased circulating lactate dehydrogenase concentration | Always |
| Myoglobinuria | Always |
| Recurrent myoglobinuria | Always |
| Dark urine | Very often (80–99%) |
| Fever | Very often (80–99%) |
| Highly elevated creatine kinase | Very often (80–99%) |
| Abnormality of glycolipid metabolism | Often (30–79%) |
| Elevated circulating aldolase concentration | Often (30–79%) |
| Exercise-induced myoglobinuria | Often (30–79%) |
| High liver enzymes | Often (30–79%) |
| High blood phosphate levels | Sometimes (5–29%) |
| Increased circulating potassium concentration | Sometimes (5–29%) |
| Low blood calcium levels | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Muscle weakness | Always |
| Type 2 muscle fiber atrophy | Often (30–79%) |
| Viral infection-induced rhabdomyolysis | Often (30–79%) |
| Fatigable weakness of swallowing muscles | Sometimes (5–29%) |
| Muscle spasm | Sometimes (5–29%) |
| Neck muscle weakness | Sometimes (5–29%) |
| Acute rhabdomyolysis | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Decreased reflex response | Always |
| Diminished deep tendon reflex | Often (30–79%) |
| Abnormal gait | Sometimes (5–29%) |
| Abnormal speech pattern | Sometimes (5–29%) |
| Absent reflexes | Not recorded |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Renal failure | Often (30–79%) |
| Acute kidney injury | Sometimes (5–29%) |
| Oliguria | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormality of jaw muscles | Sometimes (5–29%) |
| Chewing difficulties | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Lower limb muscle weakness | Sometimes (5–29%) |
| Proximal upper limb muscle weakness | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Muscle ache | Always |
| Exercise-induced muscle pain | Often (30–79%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Disseminated intravascular coagulation | Rarely (1–4%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal heart rate | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Muscle inflammation | Often (30–79%) |
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 LPIN1 and how often each is seen. Find out more at hpo.jax.org.
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