Showing entry for Ocular albinism with congenital sensorineural deafness
| General Disease Information | |
|---|---|
| BXGD Id | BXGD024079 |
| Disease Name | Ocular albinism with congenital sensorineural deafness |
| Disease CUI Id | C4750999 |
| MeSH Codes | C16 C18 C11 C17 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|