| DISEASE NAME | Disorder of sex development |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | N.A. |
| 12 combinations linked to 90771 | OLI572; OLI573; OLI574; OLI575; OLI597; OLI598; OLI599; OLI600; OLI601; OLI602; OLI603; OLI604 |
| 12 gene combinations linked to 90771 | INHA; NR5A1; AKR1C3; DOCK8; FSHR; NCOR1; NR5A1; POR; CACNG4; FBLN2; NAV1; NR5A1; SMAD6; SRA1; ZDHHC11; ZFPM2; CHD7; DENND1A; GDNF; GLI2; NR5A1; SOX30; CYP1A1; EVC; GRID1; MAMLD1; NOTCH1; RET; RIPK4; ZBTB16; MAMLD1; RECQL4; GLI2; MAMLD1; RECQL4; CDH23; COL9A3; MAML1; MAMLD1; NOTCH1; BNC2; FGF10; HSD3B2; IRX5; MAML2; MAMLD1; NOTCH2; BNC2; NRP1; PROP1; PTPN11; MAML1; MAML3; IRX5; ATF3; FRAS1; IRX6; CYP1A1; HOXA13; WDR11; EYA1; GLI3; FLNA; MAMLD1; EVC; MAML3; MAMLD1; NOTCH2; PPARGC1B; WDR11; CUL4B; DAPK1; EMX2; FREM2; IGFBP2; MAML2; MAML3; MAMLD1; MYO7A; NOTCH1; PIK3R3; TGFBI; WNT9A; WNT9B |
| ORPHANET ID | 90771 |