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59 Possible Causes for Acute Cholecystitis, Erythropoietic Porphyria

  • Acute Hepatic Porphyria

    porphyria E80.1 Porphyria cutanea tarda E80.2 Other and unspecified porphyria E80.20 Unspecified porphyria E80.21 Acute intermittent (hepatic) porphyria E80.3 Defects of[icd10data.com] 2015/16 ICD-10-CM E80.29 Other porphyria Approximate Synonyms Acute intermittent porphyria Disorder of porphyrin metabolism Erythropoietic protoporphyria Porphyria Porphyria[icd9data.com] AIP VP HCP Variegate Coproporphyria Additional relevant MeSH terms: Layout table for MeSH terms Porphyrias Porphyria, Erythropoietic Porphyrias, Hepatic Coproporphyria, Hereditary[clinicaltrials.gov]

  • Erythropoietic Protoporphyria

    […] and chronic cholecystitis Chronic liver conditions, such as scarring and fibrosis, due to liver toxicity How is Erythropoietic Protoporphyria Treated?[dovemed.com] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[ghr.nlm.nih.gov] Erythropoietic protoporphyria (EPP) is the most common of the erythropoietic porphyrias.[ncbi.nlm.nih.gov]

  • Acute Intermittent Porphyria

    There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[ncbi.nlm.nih.gov] Called also intermittent acute porphyria. congenital erythropoietic porphyria (CEP) a form of erythropoietic porphyria, with cutaneous photosensitivity leading to mutilating[medical-dictionary.thefreedictionary.com] (ADP) Porphyria Cutanea Tarda (PCT) Erythropoietic Protoporphyria (EPP) and X-Linked Protoporphyria (XLP) Congenital Erythropoietic Porphyria (CEP) Hepatoerythropoietic Porphyria[porphyriafoundation.com]

  • Hemolytic Anemia

    Recent history of septic abortion, acute cholecystitis, amniocentesis makes Clostridium perfringes likely cause of hemolytic anemia.[clinicaladvisor.com] As a result, he was diagnosed as having Congenital erythropoietic porphyria.[ncbi.nlm.nih.gov] Here, in a congenital erythropoietic porphyria mouse model, we evaluate the impact of hemolysis and regenerative anemia on hepcidin synthesis and iron metabolism.[ncbi.nlm.nih.gov]

  • Cholesterol Polyp of the Gallbladder

    ( ICD-10-CM Diagnosis Code K81 K81 Cholecystitis K81.0 Acute cholecystitis K81.1 Chronic cholecystitis K81.2 Acute cholecystitis with chronic cholecystiti...[icd10data.com] porphyria.[link.springer.com] […] wall without evidence of acute cholecystitis: non specific 53.[slideshare.net]

  • Pancreatitis

    The incidence of acute cholecystitis among the elderly is probably increasing.[ncbi.nlm.nih.gov] […] acute intermittent porphyria and erythropoietic protoporphyria.[en.wikipedia.org] Patients with a diagnostic code for acute pancreatitis, cholelithiasis, acute cholecystitis, or cholecystectomy served as the numerators for the incidence calculations.[doi.org]

  • Extrahepatic Cholestasis

    Scintigraphy also provided a correct diagnosis of acute cholecystitis in all 9 patients with surgically confirmed disease.[ncbi.nlm.nih.gov] ., thalassemia, pernicious anemia, erythropoietic porphyria, and sideroblastic anemia ) Resolving hematoma or internal hemorrhage (e.g., in trauma patients or postsurgical[amboss.com] K80.42 Calculus of bile duct with acute cholecystiti... K80.43 Calculus of bile duct with acute cholecystiti... K80.44 Calculus of bile duct with chronic cholecysti...[icd10data.com]

  • Hereditary North American Indian Childhood Cirrhosis

    List of possible causes of Yellowing or similar symptoms may include: 1 Acute Cholecystitis (yellowing of the skin) Acute Hepatitis (yellowing) Acute liver failure (yellowing[familydiagnosis.com] porphyria Gilbert syndrome, Wilson disease, Dubin-Johnson syndrome α 1 -Antitrypsin deficiency, Wilson disease, lipoatrophic diabetes Adults Gaucher disease, citrullinemia[clinicalgate.com] […] cutanea tarda type 2 , Sickle cell disease , Mitochondrial DNA depletion syndrome, hepatocerebral form Hematologic Erythropoietic protoporphyria , Hemochromatosis , Hemosiderosis[wikidoc.org]

  • Sideroblastic Anemia

    Acute cholecystitis B. Parvovirus infection C. Expansion of his lymphoma D. Sickle cell vaso-occlusive crisis E.[med-ed.virginia.edu] Congenital erythropoietic porphyria (CEP), an autosomal recessive disorder, results from the markedly deficient activity of uroporphyrinogen III synthase [UROS] (also known[ommbid.mhmedical.com] One example that includes porphyria is the GATA1 erythroid transcription factor, where different mutations can lead to thalassemia, macrothrombocytopenia, or congenital erythropoietic[haematologica.org]

  • Hypochromic Microcytic Anemia with Iron Overload Type 2

    Acute cholecystitis B. Parvovirus infection C. Expansion of his lymphoma D. Sickle cell vaso-occlusive crisis E.[med-ed.virginia.edu] Erythropoietic protoporphyria, X-linked dominant (XLDPT) [MIM:300752]: A form of porphyria.[genecards.org] Defects in the UROS gene are associated with the autosomal recessive erythroid porphyria called congenital erythropoietic porphyria, CEP In the Figure below you can place[themedicalbiochemistrypage.org]

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