| DISEASE NAME | Syndrome with 46,XY disorder of sex development |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | N.A. |
| 25 combinations linked to 98087 | OLI1557; OLI1558; OLI1559; OLI1560; OLI1561; OLI1562; OLI1563; OLI1564; OLI1565; OLI1566; OLI1567; OLI1568; OLI1569; OLI1570; OLI1571; OLI1572; OLI1573; OLI1574; OLI1575; OLI1576; OLI1577; OLI1578; OLI1579; OLI1580; OLI1581 |
| 25 gene combinations linked to 98087 | HSD17B6; NR5A1; PROK2; SEMA3F; FGFR3; FLNA; GLI2; GPRC6A; NR5A1; PROKR2; FGFR1; GHR; AMH; SLC29A3; GPRC6A; KAT6B; ATP7B; COL1A1; GPC3; HSD17B3; RXFP2; AKR1C4; GPRC6A; MAP3K1; ROR2; SLC29A3; AR; FGFR1; FANCB; GHRHR; HOXA13; KAT6B; OFD1; SRA1; CACNA1F; MPDZ; SRA1; BBS7; GPRC6A; PROKR2; NR0B1; SOX8; SRA1; AMH; DHX37; MYRF; NGLY1; AR; FLNA; GPRC6A; ROR2; GLI3; POR; HSD17B6; LHX3; PTCH1; RXFP2; CHD7; SLC29A3; CTU2; GLI3; DCAF17; FEZF1; GLI3; MAMLD1; FANCD2; SLC29A3; MAMLD1; NRAS; RXFP2; SHH; GHR; NIPBL; AMH; FGFR3; SRA1; GPC3; PRKAR1A |
| ORPHANET ID | 98087 |