Pancreatic islet-cell hyperplasia
Symptom Information:
Symptom ID: | HPO:0004510 | |||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the pancreas(HPO:0001732) Abnormality of pancreas physiology(HPO:0012091) Abnormality of endocrine pancreas physiology(HPO:0012093) Abnormality of the pancreatic islet cells(HPO:0006476) Pancreatic islet-cell hyperplasia(HPO:0004510) MedDRA: |
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Database Frequency: | 9 / 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) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Exercise-induced hyperinsulinism | (Orphanet:165991) |
Greenberg dysplasia | (Orphanet:1426) |
Leprechaunism | (Orphanet:508) |
Perlman syndrome | (Orphanet:2849) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Tyrosinemia type 1 | (Orphanet:882) |