Showing entry for Charcot-Marie-Tooth disease and deafness
| General Disease Information | |
|---|---|
| BXGD Id | BXGD016063 |
| Disease Name | Charcot-Marie-Tooth disease and deafness |
| Disease CUI Id | C1861669 |
| MeSH Codes | C23 C16 C10 C09 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Otorhinolaryngologic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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