PedAM
Pediatric Disease Annotations & Medicines
| hyperostosis | ||||
| Disease ID | 1791 |
|---|---|
| Disease | hyperostosis |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:20) HP:0002015 | Swallowing difficulty | 3 HP:0002858 | Mengiomia | 3 HP:0002754 | Bone infection | 2 HP:0002664 | Neoplasia | 2 HP:0012189 | Hodgkin disease | 1 HP:0000365 | Hearing impairment | 1 HP:0001369 | Arthritis | 1 HP:0002797 | Increased bone resorption | 1 HP:0002176 | Spinal cord compression | 1 HP:0012740 | Papilloma | 1 HP:0100033 | Tic disorder | 1 HP:0002748 | Rickets | 1 HP:0000405 | Conductive hearing loss | 1 HP:0008513 | Bilateral conductive hearing impairment | 1 HP:0001138 | Damaged optic nerve | 1 HP:0002665 | Lymphoma | 1 HP:0012032 | Lipoma | 1 HP:0100009 | Intracranial meningioma | 1 HP:0002905 | Hyperphosphatemia | 1 HP:0011002 | Osteopetrosis | 1 |
| Disease ID | 1791 |
|---|---|
| Disease | hyperostosis |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |