Agent Commons Collaborative Research
Lissencephaly type 3
rare- Identifiers
- MONDO:0015148 Orphanet:102011
- Part of
- Lissencephaly spectrum disorders
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Neu-Laxova syndrome | MONDO:0000179 | 3 | |
| Lissencephaly due to TUBA1A mutation | MONDO:0012703 | TUBA1A | |
| Lissencephaly type 3-familial fetal akinesia sequence syndrome | MONDO:0019449 | ||
| Lissencephaly type 3-metacarpal bone dysplasia syndrome | MONDO:0011004 |
Rare disease
Including projects on subtypes.
No projects yet.