Disease #00091 (HP (Hereditary Pancreatitis), OMIM:167800)

Official abbreviation HP
Name Hereditary Pancreatitis
OMIM ID 167800
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene PRSS1
Associated tissues pancreas
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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Owner     
00000533 Kek Heng Chua et al.(2011) M Malaysia Chinese - - - HP abdomen CT scan showed pancreatic duct stones with distal duct dilatation and parenchymal calcification PRSS1 PRSS1 2 1 Nur Aisyah Athirah
00000635 Kek Heng Chua et al.(2011) M Malaysia Chinese - - - HP - PRSS1 PRSS1 2 1 Nur Aisyah Athirah
00000636 Kek Heng Chua et al.(2011) F Malaysia Chinese - - - HP CT scan showed pancreatic calcifications PRSS1 PRSS1 2 1 Nur Aisyah Athirah
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