Pancreatic islet-cell hyperplasia

Symptom Information:

Symptom ID: HPO:0004510
Synonyms:
Hyperplastic islets of langerhans [HPO:0004510]
Hypertrophic pancreatic islets [HPO:0004510]
Islet of Langerhans hyperplasia [HPO:0004510]
Islets of langerhans hypertrophy [HPO:0004510]
Hyperplastic islets of Langerhans [OMIM:Hyperplastic islets of Langerhans]
Hypertrophic pancreatic islets [OMIM:Hypertrophic pancreatic islets]
Islets of Langerhans hypertrophy [OMIM:Islets of Langerhans hypertrophy]
Pancreatic islet-cell hypertrophy [OMIM:Pancreatic islet-cell hypertrophy]
Islets of Langerhans hyperplasia [OMIM:Islets of Langerhans hyperplasia]
Quality:
Cross references:
OMIM: "Hyperplastic islets of Langerhans" [OMIM:Hyperplastic islets of Langerhans]
OMIM: "Hypertrophic pancreatic islets" [OMIM:Hypertrophic pancreatic islets]
OMIM: "Islets of Langerhans hypertrophy" [OMIM:Islets of Langerhans hypertrophy]
OMIM: "Pancreatic islet-cell hypertrophy" [OMIM:Pancreatic islet-cell hypertrophy]
OMIM: "Islets of Langerhans hyperplasia" [OMIM:Islets of Langerhans hyperplasia]
Is a (Direct Parents):
HPO         Abnormality of the pancreatic islet cells
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:
Database Frequency: 9 / 7739
Resource:

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)