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Summary Literature (0)
MIM:616263 - NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1; IMNEPD1

Xenbase Genes: ptrh2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014554 - obsolete infantile multisystem neurologic-endocrine-pancreatic disease
MONDO:8000012 - neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1