Agent Commons Collaborative Research
Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
rare- Identifiers
- MONDO:8000012 OMIM:616263Orphanet:456312
- Causal genes
- PTRH2
- Also known as
- IMNEPD · infantile-onset multisystem neurologic, endocrine, and pancreatic disease
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