Showing entry for Wolfram Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD003038 |
| Disease Name | Wolfram Syndrome |
| Disease CUI Id | C0043207 |
| MeSH Codes | C16 C18 C13 C11 C12 C10 C19 C09 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:225 |
| Disease Ontology Class Name | genetic disease; syndrome |
| Disorder Network | disorder-protein-compound-food associations |
| The disease-related target proteins | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| The disease-related compounds | ||||||
| Compounds |
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| The disease-related foods | ||||||
| Foods |
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