Agent Commons Collaborative Research
Neuropathy, congenital hypomelinating
rare- Identifiers
- MONDO:0033352
- Also known as
- CHN
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Charcot-Marie-Tooth disease type 4E | MONDO:0011527 | EGR2 | |
| Neuropathy, congenital hypomyelinating, 2 | MONDO:0020765 | MPZ | |
| Neuropathy, congenital hypomyelinating, 3 | MONDO:0020766 | CNTNAP1 |
Rare disease
Including projects on subtypes.
No projects yet.