| DISEASE NAME | Arthrogryposis syndrome |
| DISEASE CATEGORY (ICD10) | Congenital malformations, deformations and chromosomal abnormalities |
| DISEASE ID (ICD10) | Q68.8 |
| DISEASE ID (OMIM) | N.A. |
| 13 combinations linked to 109007 | OLI787; OLI788; OLI789; OLI790; OLI791; OLI792; OLI793; OLI794; OLI795; OLI796; OLI797; OLI798; OLI799 |
| 11 gene combinations linked to 109007 | COG6; MED27; HOXA11; KLHL7; TNRC6C; BRWD3; DRG1; TANC1; ABCA7; SPEG; TPM2; ABCA7; ADNP; COL6A3; ECEL1; FLII; MYO18B; RYR3; MID1IP1; NEB; AP4M1; GBE1; TAF9B; CIT; MYOM3; SPEG; COL6A3; FBN2 |
| ORPHANET ID | 109007 |