Abnormality of pancreas morphology

Symptom Information:

Symptom ID: HPO:0012090
Pancreas structural anomaly [Orphanet:30000]
Structural anomalies of the pancreas [Orphanet:30000]
Cross references:
Orphanet:30000 "Structural anomalies of the pancreas" [Orphanet:30000]
Is a (Direct Parents):
HPO         Abnormality of the pancreas
Is a (Whole tree): HPO:
    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)
Database Frequency: 31 / 7739

All diseases associated with this symptom:

Annular pancreas (Orphanet:675)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Beckwith-Wiedemann syndrome (Orphanet:116)
Bohring-Opitz syndrome (Orphanet:97297)
Campomelia, Cumming type (Orphanet:1318)
Cartilage-hair hypoplasia (Orphanet:175)
Congenital atransferrinemia (Orphanet:1195)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cystic fibrosis (Orphanet:586)
Diabetic embryopathy (Orphanet:1926)
Duodenal atresia (Orphanet:1203)
Isolated polycystic liver disease (Orphanet:2924)
Johanson-Blizzard syndrome (Orphanet:2315)
Maturity-onset diabetes of the young, type 8, with exocrine dysfunction (OMIM:609812)
Multiple endocrine neoplasia type 1 (Orphanet:652)
NPHP3-related Meckel-like syndrome (Orphanet:3032)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Partial pancreatic agenesis (Orphanet:2805)
Pearson syndrome (Orphanet:699)
Perlman syndrome (Orphanet:2849)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Short rib-polydactyly syndrome (Orphanet:1505)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
Shwachman-Diamond syndrome (Orphanet:811)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Tracheo-esophageal fistula - hypospadias (Orphanet:2042)
Triploidy (Orphanet:3376)
Tuberous sclerosis (Orphanet:805)
VACTERL/VATER association (Orphanet:887)
Von Hippel-Lindau disease (Orphanet:892)
Young syndrome (Orphanet:3471)