Showing entry for Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014072 |
| Disease Name | Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome |
| Disease CUI Id | C1836033 |
| MeSH Codes | C16 C17 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 |
| Disease Ontology Class Name | genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|