Showing entry for HYPERTRICHOSIS, CONGENITAL GENERALIZED
| General Disease Information | |
|---|---|
| BXGD Id | BXGD015559 |
| Disease Name | HYPERTRICHOSIS, CONGENITAL GENERALIZED |
| Disease CUI Id | C1855900 |
| MeSH Codes | C16 C17 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0001574 |
| Human Phenotype Ontology Term | Abnormality of the integument |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|