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:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | C14ORF39 CL E G H | 317761 | 19849 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | CCDC34 CL E G H | 91057 | 25079 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | CFTR CL E G H | 1080 | 1884 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 1371 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | CHD7 CL E G H | 55636 | 20626 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 515 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DAZ1 CL E G H | 1617 | 2682 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DAZ2 CL E G H | 57055 | 15964 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DAZ3 CL E G H | 57054 | 15965 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DAZ4 CL E G H | 57135 | 15966 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DDX3Y CL E G H | 8653 | 2699 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | DUSP6 CL E G H | 1848 | 3072 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | FANCM CL E G H | 57697 | 23168 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 107 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | FGF17 CL E G H | 8822 | 3673 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 3 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | FGF8 CL E G H | 2253 | 3686 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 17 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | FGFR1 CL E G H | 2260 | 3688 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 172 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | GNRH1 CL E G H | 2796 | 4419 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 15 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | GNRHR CL E G H | 2798 | 4421 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 92 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | HS6ST1 CL E G H | 9394 | 5201 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 8 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | KISS1 CL E G H | 3814 | 6341 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 3 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | KISS1R CL E G H | 84634 | 4510 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 14 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | KLHL10 CL E G H | 317719 | 18829 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 3 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | MEIOB CL E G H | 254528 | 28569 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | MEIOB CL E G H | 254528 | 28569 | OMIM:617706 | Spermatogenic failure 22 | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | MOV10L1 CL E G H | 54456 | 7201 | OMIM:619878 | | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | MSH4 CL E G H | 4438 | 7327 | OMIM:108420 | Spermatogenic failure 2 | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | MSH5 CL E G H | 4439 | 7328 | OMIM:619937 | | | | | 5 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | NANOS1 CL E G H | 340719 | 23044 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | NANOS1 CL E G H | 340719 | 23044 | ORPHA:399808 | Male infertility with teratozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | NR5A1 CL E G H | 2516 | 7983 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 38 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | NSMF CL E G H | 26012 | 29843 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 6 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | PNLDC1 CL E G H | 154197 | 21185 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | PNLDC1 CL E G H | 154197 | 21185 | OMIM:619528 | SPERMATOGENIC FAILURE 57; SPGF57 | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | PROK2 CL E G H | 60675 | 18455 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 9 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | PROKR2 CL E G H | 128674 | 15836 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 34 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | RBMY1A1 CL E G H | 5940 | 9912 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | RNF212 CL E G H | 285498 | 27729 | OMIM:619673 | SPERMATOGENIC FAILURE 62; SPGF62 | | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SHOC1 CL E G H | 158401 | 26535 | OMIM:619949 | | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SOHLH1 CL E G H | 402381 | 27845 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 3 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SPRY4 CL E G H | 81848 | 15533 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 5 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | STAG3 CL E G H | 10734 | 11356 | OMIM:619672 | SPERMATOGENIC FAILURE 61; SPGF61 | | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SYCE1 CL E G H | 93426 | 28852 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SYCE1 CL E G H | 93426 | 28852 | OMIM:616950 | Spermatogenic failure 15 | | | | 4 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | SYCP3 CL E G H | 50511 | 18130 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 12 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TAC3 CL E G H | 6866 | 11521 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 6 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TACR3 CL E G H | 6870 | 11528 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 34 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TAF4B CL E G H | 6875 | 11538 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 1 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TDRD9 CL E G H | 122402 | 20122 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TERB1 CL E G H | 283847 | 26675 | OMIM:619646 | SPERMATOGENIC FAILURE 60; SPGF60 | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TERB2 CL E G H | 145645 | 28520 | OMIM:619645 | SPERMATOGENIC FAILURE 59; SPGF59 | | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TEX11 CL E G H | 56159 | 11733 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 5 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TEX14 CL E G H | 56155 | 11737 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 1 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TEX15 CL E G H | 56154 | 11738 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 1 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | TSPY1 CL E G H | 7258 | 12381 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | USP9Y CL E G H | 8287 | 12633 | ORPHA:1646 | Partial chromosome Y deletion | HP:0040281 - Very frequent | | | 2 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | WDR11 CL E G H | 55717 | 13831 | ORPHA:432 | Normosmic congenital hypogonadotropic hypogonadism | HP:0040281 - Very frequent | | | 10 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | XRCC2 CL E G H | 7516 | 12829 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 125 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | ZMYND15 CL E G H | 84225 | 20997 | ORPHA:399805 | Male infertility with azoospermia or oligozoospermia due to single gene mutation | HP:0040281 - Very frequent | | | 1 | | |
HP:0011961 | HP:0011961 | Non-obstructive azoospermia | 0 | ZSWIM7 CL E G H | 125150 | 26993 | OMIM:619831 | SPERMATOGENIC FAILURE 71; SPGF71 | | | | | | |