Aplasia/Hypoplasia of the pancreas

Symptom Information:

Symptom ID: HPO:0100800
Synonyms:
Congenital aplasia of pancreas [Orphanet:30110]
Congenital absence of pancreas (disorder) [Orphanet:30110]
Congenital absence of pancreas [Orphanet:30110]
Congenital absence/agenesis/aplasia/hypoplasia of the pancreas [Orphanet:30110]
Quality:
Cross references:
Orphanet:30110 "Congenital absence/agenesis/aplasia/hypoplasia of the pancreas" [Orphanet:30110]
UMLS:C0266266 "Congenital absence of pancreas" [Orphanet:30110]
Is a (Direct Parents):
Orphanet Abnormality of pancreas morphology
HPO         Abnormal pancreas size
Orphanet Pancreatic hypoplasia
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 morphology(HPO:0012090)
                   Abnormal pancreas size(HPO:0012094)
                      Aplasia/Hypoplasia of the pancreas(HPO:0100800)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
Matthew-Wood syndrome (Orphanet:2470)
Maturity-onset diabetes of the young, type 4 (OMIM:606392)
Pancreatic agenesis, congenital (OMIM:260370)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Renal cysts and diabetes syndrome (Orphanet:93111)
Wolcott-Rallison syndrome (Orphanet:1667)