Showing entry for HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
| General Disease Information | |
|---|---|
| BXGD Id | BXGD017216 |
| Disease Name | HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) |
| Disease CUI Id | C2673630 |
| MeSH Codes | C16 C05 C19 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System 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
|