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:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | FANCD2 CL E G H | 2177 | 3585 | OMIM:227646 | Fanconi anemia, complementation group D2 | | | | 147 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040282 - Frequent | | | 111 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | LMBR1 CL E G H | 64327 | 13243 | ORPHA:93321 | Radial hemimelia | HP:0040281 - Very frequent | | | 106 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | SHH CL E G H | 6469 | 10848 | ORPHA:93321 | Radial hemimelia | HP:0040281 - Very frequent | | | 67 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | TRIO CL E G H | 7204 | 12303 | ORPHA:476126 | Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome | HP:0040283 - Occasional | | | 8 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040282 - Frequent | | | 6 | | |
HP:0010035 | HP:0010035 | Aplasia of the 1st metacarpal | 0 | XRCC2 CL E G H | 7516 | 12829 | OMIM:617247 | FANCONI ANEMIA, COMPLEMENTATION GROUP U | | | | 125 | | |