Showing entry for Congenital hemihypertrophy
| General Disease Information | |
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| BXGD Id | BXGD006909 |
| Disease Name | Congenital hemihypertrophy |
| Disease CUI Id | C0332890 |
| 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 | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0040064 HP:0001507 |
| Human Phenotype Ontology Term | Abnormality of limbs; Growth abnormality |
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| Disorder Network | disorder-protein-compound-food associations |
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