Showing entry for Vitamin D Hydroxylation-Deficient Rickets, Type 1B
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014332 |
| Disease Name | Vitamin D Hydroxylation-Deficient Rickets, Type 1B |
| Disease CUI Id | C1838657 |
| MeSH Codes | C16 C18 C13 C05 C12 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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