Showing entry for Severe intrauterine growth retardation
| General Disease Information | |
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| BXGD Id | BXGD015551 |
| Disease Name | Severe intrauterine growth retardation |
| Disease CUI Id | C1855843 |
| MeSH Codes | C23 C16 C13 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| Semantic Type | Finding |
| Human Phenotype Ontology Id | HP:0001507 |
| Human Phenotype Ontology Term | Growth abnormality |
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| Disorder Network | disorder-protein-compound-food associations |
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