Islet cell hyperplasia, diffuse
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 7 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276580) |
Autosomal dominant hyperinsulinism due to SUR1 deficiency | (Orphanet:276575) |
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency | (Orphanet:79644) |
Autosomal recessive hyperinsulinism due to SUR1 deficiency | (Orphanet:79643) |
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276603) |
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency | (Orphanet:276598) |
Exercise-induced hyperinsulinism | (Orphanet:165991) |