Showing entry for Congenital neutropenia, myelofibrosis, nephromegaly syndrome
| General Disease Information | |
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| BXGD Id | BXGD024086 |
| Disease Name | Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
| Disease CUI Id | C4755251 |
| MeSH Codes | C16 C15 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| Semantic Type | Disease or Syndrome |
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| Disorder Network | disorder-protein-compound-food associations |
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