Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Hypolysinemia
Always present (100%)HP:0500142
Mental and motor retardation
Always present (100%)HP:0001263
Poor weight gain
Very frequent (80-99%)HP:0001508
Protein avoidance
Very frequent (80-99%)HP:0002038
Abnormal circulating serine concentration
Frequent (30-79%)HP:0012278
Alveolar proteinosis
Frequent (30-79%)HP:0006517
Bleeding tendency
Frequent (30-79%)HP:0001892
Bone marrow hypercellularity
Frequent (30-79%)HP:0031020
Cirrhosis
Frequent (30-79%)HP:0001394
CKD
Frequent (30-79%)HP:0012622
Cognitive deficits
Frequent (30-79%)HP:0100543
Decreased glomerular filtration rate
Frequent (30-79%)HP:0012213
Decreased haemoglobin
Frequent (30-79%)HP:0001903
Decreased HDL cholesterol concentration
Frequent (30-79%)HP:0003233
Delayed skeletal development
Frequent (30-79%)HP:0002750
Diarrhea
Frequent (30-79%)HP:0002014
Elevated plasma citrulline
Frequent (30-79%)HP:0011966
Elevated serum transaminases
Frequent (30-79%)HP:0002910
Elevated total cholesterol
Frequent (30-79%)HP:0003124
Enlarged liver
Frequent (30-79%)HP:0002240
Fat in feces
Frequent (30-79%)HP:0002570
Feeding difficulties
Frequent (30-79%)HP:0011968
Glomerulonephritis
Frequent (30-79%)HP:0000099
Growth deficiency
Frequent (30-79%)HP:0001510
Hemophagocytosis
Frequent (30-79%)HP:0012156
Hepatic failure
Frequent (30-79%)HP:0001399
Hepatosplenomegaly
Frequent (30-79%)HP:0001433
High blood ammonia levels
Frequent (30-79%)HP:0001987
High plasma glutamine
Frequent (30-79%)HP:0003217
High urine arginine levels
Frequent (30-79%)HP:0003268
Quick Facts
- SNOMED CT
- 303852004
- UMLS CUI
- C0268647
- Fully Specified Name
- Lysinuric protein intolerance (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.