c syndrome |
Disease ID | 548 |
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Disease | c syndrome |
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:1) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs119477056 | NA | 10225 | CD96 | umls:C0796095 | CLINVAR | NA | 0.480271442 | NA | CD96 | 3 | 111585362 | C | A,T |
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:1) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0004209 | Clinodactyly of the 5th finger | MP:0003694 | failure of blastocyst to hatch from the zona pellucida;HP:0000175 | Cleft palate |
Mapped by homologous gene(Total Items:1) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0002650 | Scoliosis | MP:0010465 | aberrant origin of the right subclavian artery;HP:0000243 | Trigonocephaly |
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.) |