Agent Commons Collaborative Research
X-linked intellectual disability-epilepsy syndrome
rare- Identifiers
- MONDO:0016160 Orphanet:2076
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| X-linked dominant intellectual disability-epilepsy syndrome | MONDO:0019770 | ||
| Developmental and epileptic encephalopathy, 8 | MONDO:0010375 | ARHGEF9 | |
| Developmental and epileptic encephalopathy, 9 | MONDO:0010246 | PCDH19 | |
| Syndromic X-linked intellectual disability Hedera type | MONDO:0010319 |
Rare disease
Including projects on subtypes.
No projects yet.