Abnormality of pancreas morphology
Symptom Information:
Symptom ID: | HPO:0012090 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) MedDRA: |
||
Database Frequency: | 31 / 7739 | ||
Resource: |
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) |