Pancreatic colipase deficiency




Input patient's signs and symptoms


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Total: 0 (papers)
  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 7

HPO ID Term Frequency
HP:0001738 Exocrine pancreatic insufficiency Very frequent (99-80%)
HP:0001889 Megaloblastic anemia Very frequent (99-80%)
HP:0002028 Chronic diarrhea Very frequent (99-80%)
HP:0002570 Steatorrhea Very frequent (99-80%)
HP:0002630 Fat malabsorption Very frequent (99-80%)
HP:0001081 Cholelithiasis Occasional (29-5%)
HP:0001510 Growth delay Excluded (0%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID