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infantile multisystem neurologic-endocrine-pancreatic disease

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A progressive multisystem disease characterized by a variety of neurologic, endocrine, and, in some patients, pancreatic features. Variable clinical symptoms include global developmental delay, hypotonia, hearing loss, ataxia, hyporeflexia, facial dysmorphism, hypothyroidism, and pancreatic insufficiency.
Mondo Term and Equivalent IDs
MONDO:0014554:  infantile multisystem neurologic-endocrine-pancreatic disease
Orphanet:456312: 
UMLS:C4015728: