Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | AKT1 CL E G H | 207 | 391 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 54 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040281 - Very frequent | | | 9 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040281 - Very frequent | | | 58 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | HRAS CL E G H | 3265 | 5173 | OMIM:188470 | Thyroid cancer, nonmedullary, 2 | . | | | 113 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | KLLN CL E G H | 100144748 | 37212 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040281 - Very frequent | | | 3 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | MINPP1 CL E G H | 9562 | 7102 | OMIM:188470 | Thyroid cancer, nonmedullary, 2 | . | | | 3 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | NRAS CL E G H | 4893 | 7989 | OMIM:188470 | Thyroid cancer, nonmedullary, 2 | . | | | 102 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | PDE11A CL E G H | 50940 | 8773 | ORPHA:1359 | Carney complex | | | | 13 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 162 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | PRKAR1A CL E G H | 5573 | 9388 | ORPHA:1359 | Carney complex | | | | 134 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | PTEN CL E G H | 5728 | 9588 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 948 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 237 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | SDHC CL E G H | 6391 | 10682 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 147 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 129 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | SEC23B CL E G H | 10483 | 10702 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 60 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | SRGAP1 CL E G H | 57522 | 17382 | OMIM:188470 | Thyroid cancer, nonmedullary, 2 | . | | | 3 | | |
HP:0006731 | HP:0006731 | Follicular thyroid carcinoma | 0 | USF3 CL E G H | 205717 | 30494 | ORPHA:201 | Cowden syndrome | HP:0040283 - Occasional | | | 1 | | |