Human Phenotype Ontology 
Grandparent Node:
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Abnormality of pancreas physiology (HP:0012091)help
Grandparent Node:
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Increased inflammatory response (HP:0012649)help
Parent Node:
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Pancreatitis (HP:0001733)help
..Starting node
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Recurrent pancreatitis (HP:0100027)help
Term ID: 100027
Name: Recurrent pancreatitis
Synonym: Recurring pancreas inflammation; Recurring pancreatitis
Definition: A recurrent form of pancreatitis.
Comments:
Reference: HP:0100027
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute pancreatitis (HP:0001735) help
..expandChronic calcifying pancreatitis (HP:0005236) help
..expandChronic pancreatitis (HP:0006280) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100027HP:0100027Recurrent pancreatitis0CASR CL E G H8461514ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent272
HP:0100027HP:0100027Recurrent pancreatitis0CAV1 CL E G H8571527OMIM:606721Lipodystrophy, familial partial, type 711
HP:0100027HP:0100027Recurrent pancreatitis0CDC73 CL E G H7957716783OMIM:145001Hyperparathyroidism 2.169
HP:0100027HP:0100027Recurrent pancreatitis0CFTR CL E G H10801884ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent1371
HP:0100027HP:0100027Recurrent pancreatitis0COX1 CL E G H45127419ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0COX2 CL E G H45137421ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0COX3 CL E G H45147422ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0CPA1 CL E G H13572296ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent5
HP:0100027HP:0100027Recurrent pancreatitis0CTRC CL E G H113302523ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent39
HP:0100027HP:0100027Recurrent pancreatitis0GCGR CL E G H26424192OMIM:619290MAHVASH DISEASE; MVAH1
HP:0100027HP:0100027Recurrent pancreatitis0GPIHBP1 CL E G H33832824945OMIM:615947Hyperlipoproteinemia, type ID12
HP:0100027HP:0100027Recurrent pancreatitis0ND1 CL E G H45357455ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0ND4 CL E G H45387459ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0ND5 CL E G H45407461ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0ND6 CL E G H45417462ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0PRSS1 CL E G H56449475ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent51
HP:0100027HP:0100027Recurrent pancreatitis0PRSS2 CL E G H56459483ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent1
HP:0100027HP:0100027Recurrent pancreatitis0SPINK1 CL E G H669011244ORPHA:676Hereditary chronic pancreatitisHP:0040281 - Very frequent34
HP:0100027HP:0100027Recurrent pancreatitis0TRNF CL E G H45587481ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNH CL E G H45647487ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNL1 CL E G H45677490ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNQ CL E G H45727495ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNS1 CL E G H45747497ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNS2 CL E G H45757498ORPHA:550MELASHP:0040283 - Occasional
HP:0100027HP:0100027Recurrent pancreatitis0TRNW CL E G H45787501ORPHA:550MELASHP:0040283 - Occasional


Genes (25) :CASR CAV1 CDC73 CFTR COX1 COX2 COX3 CPA1 CTRC GCGR GPIHBP1 ND1 ND4 ND5 ND6 PRSS1 PRSS2 SPINK1 TRNF TRNH TRNL1 TRNQ TRNS1 TRNS2 TRNW

Diseases (6) :ORPHA:676 OMIM:606721 OMIM:145001 ORPHA:550 OMIM:619290 OMIM:615947
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.