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:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | CDC73 CL E G H | 79577 | 16783 | OMIM:145001 | Hyperparathyroidism 2 | . | | | 169 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | FH CL E G H | 2271 | 3700 | ORPHA:523 | Hereditary leiomyomatosis and renal cell cancer | | | | 301 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 9 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 58 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:363618 | LMNA-related cardiocutaneous progeria syndrome | HP:0040281 - Very frequent | | | 645 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | MET CL E G H | 4233 | 7029 | OMIM:605074 | RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1 | | | | 375 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 3 | | |
HP:0006766 | HP:0006766 | Papillary renal cell carcinoma | 0 | PRCC CL E G H | 5546 | 9343 | OMIM:605074 | RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1 | | | | | | |
HP:0006766 | HP:0011797 | Papillary renal cell carcinoma type 1 | 1 | CL E G H | | | | | | | | | | |
HP:0006766 | HP:0006732 | Papillary renal cell carcinoma type 2 | 1 | FH CL E G H | 2271 | 3700 | ORPHA:523 | Hereditary leiomyomatosis and renal cell cancer | HP:0040283 - Occasional | | | 301 | | |