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Traits
Traits linked to LPIN2
lipin 2
The Human Phenotype Ontology links 44 traits to LPIN2, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Erythroid hyperplasia | Always |
| Bone marrow disease | Very often (80–99%) |
| Congenital hypoplastic anemia | Very often (80–99%) |
| Hypochromic microcytic anemia | Very often (80–99%) |
| Elevated white blood count | Often (30–79%) |
| Microcytic anemia | Often (30–79%) |
| Anemia of inadequate production | Not recorded |
| Decreased mean corpuscular volume | Not recorded |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Episodic fever | Always |
| High ESR | Always |
| Joint swelling | Always |
| Fever | Very often (80–99%) |
| Fluid retention | Often (30–79%) |
| High urine protein levels | Sometimes (5–29%) |
| Small amount of blood in urine | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Abnormal inflammatory response | Very often (80–99%) |
| Bone infection | Very often (80–99%) |
| Pimple | Very often (80–99%) |
| Acne | Often (30–79%) |
| Skin rash | Often (30–79%) |
| Inflammatory abnormality of the skin | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Bone pain | Always |
| Delayed bone maturation | Always |
| Increased bone mineral density | Often (30–79%) |
| Synovitis | Often (30–79%) |
| Flexed joint that cannot be straightened | Sometimes (5–29%) |
| Increased susceptibility to fractures | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Always |
| Wasting syndrome | Very often (80–99%) |
| Weight loss | Very often (80–99%) |
| Growth delay | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Enlarged liver and spleen | Very often (80–99%) |
| Increased spleen size | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Enlarged liver | Often (30–79%) |
| Malabsorption | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Cough | Sometimes (5–29%) |
| Lung infiltrates | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Joint pain | Always |
| Muscle ache | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Irregular wide portion of a long bone | Very often (80–99%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Delayed puberty | Often (30–79%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Glomerulopathy | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Papule | Very often (80–99%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Headache | 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 LPIN2 and how often each is seen. Find out more at hpo.jax.org.
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