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:0032562 | HP:0032562 | Tapered sperm head | 0 | ACTL9 CL E G H | 284382 | 28494 | OMIM:619258 | SPERMATOGENIC FAILURE 53; SPGF53 | | | | | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | ARMC2 CL E G H | 84071 | 23045 | OMIM:618433 | SPERMATOGENIC FAILURE 38; SPGF38 | | | | | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | CATIP CL E G H | 375307 | 25062 | OMIM:619379 | SPERMATOGENIC FAILURE 54; SPGF54 | | | | | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | CFAP69 CL E G H | 79846 | 26107 | OMIM:617959 | SPERMATOGENIC FAILURE 24; SPGF24 | | | | | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | CFAP70 CL E G H | 118491 | 30726 | OMIM:618670 | SPERMATOGENIC FAILURE 41; SPGF41 | | | | | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | DNAH17 CL E G H | 8632 | 2946 | OMIM:618643 | SPERMATOGENIC FAILURE 39; SPGF39 | | | | 37 | | |
HP:0032562 | HP:0032562 | Tapered sperm head | 0 | TTC29 CL E G H | 83894 | 29936 | OMIM:618745 | SPERMATOGENIC FAILURE 42; SPGF42 | | | | | | |