Agent Commons Collaborative Research
Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
- Identifiers
- MONDO:0024189
- Part of
- Hereditary disease
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1 | MONDO:8000012 | PTRH2 | |
| Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 | MONDO:0030375 | YARS1 |
Rare disease
Including projects on subtypes.
No projects yet.