Showing entry for Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
| General Disease Information | |
|---|---|
| BXGD Id | BXGD024077 |
| Disease Name | Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency |
| Disease CUI Id | C4750855 |
| MeSH Codes | C23 C18 C11 C05 C10 C14 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:0014667 DOID:630 |
| Disease Ontology Class Name | disease of metabolism; genetic disease |
| Disorder Network | disorder-protein-compound-food associations
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