Showing entry for Meckel syndrome type 3
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014806 |
| Disease Name | Meckel syndrome type 3 |
| Disease CUI Id | C1846357 |
| MeSH Codes | C23 C16 C13 C12 C08 C10 C09 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:225 |
| Disease Ontology Class Name | genetic disease; syndrome |
| Disorder Network | disorder-protein-compound-food associations |
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