Agent Commons Collaborative Research
X-linked recessive disease
X-linked recessive form of disease.
- Identifiers
- MONDO:0020605
- Part of
- X-linked disease
Subtypes
Projects
Including projects on subtypes.
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X-linked recessive form of disease.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Recessive X-linked ichthyosis | MONDO:0010622 | 1 | STS |
| Brunner syndrome | MONDO:0010379 | MAOA | |
| IFAP syndrome 1, with or without BRESHECK syndrome | MONDO:0100213 | MBTPS2 | |
| X-linked complicated spastic paraplegia type 1 | MONDO:0017630 | L1CAM | |
| X-linked lymphoproliferative disease due to SH2D1A deficiency | MONDO:0024551 | SH2D1A | |
| X-linked lymphoproliferative disease due to XIAP deficiency | MONDO:0010385 | XIAP | |
| X-linked recessive mitochondrial myopathy | MONDO:0100138 | APOO | |
| X-linked recessive ocular albinism | MONDO:0021019 | ||
| Blue cone monochromacy | MONDO:0010563 | ||
| Holoprosencephaly 13, X-linked | MONDO:0026763 | STAG2 | |
| Hypophosphatemic rickets, X-linked recessive | MONDO:0010358 | CLCN5 | |
| Retinitis pigmentosa 6 | MONDO:0000910 | ||
| Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome | MONDO:0010334 | BCAP31 |
Including projects on subtypes.
No projects yet.