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3,047 Possible Causes for Abnormal Corticomedullary Differentiation, Gastric Adenocarcinoma, Retinal Degeneration

  • Ataxia Telangiectasia

    […] to lead to the development of gastric adenocarcinoma.[ncbi.nlm.nih.gov] Björklund, Markus Ringnér, Thomas Perlmann & Johan Holmberg Nature Communications (2018) DZNep inhibits H3K27me3 deposition and delays retinal degeneration in the rd1 mice[doi.org] Cellular immunity can also be affected in A-T: abnormal development of the thymus, with absence of Hassall's corpuscles and corticomedullary differentiation, impaired delayed[err.ersjournals.com]

  • Pernicious Anemia

    Gastric adenocarcinoma infiltrating the gastric cardia was seen on gastroscopy.[ncbi.nlm.nih.gov] Clinically, vitamin E deficiency causes a sensory peripheral neuropathy, ataxia, retinitis pigmentosa, and skeletal and cardiac myopathy.[neuropathology-web.org] Gastric adenocarcinoma occurred in 1.7% of patients after a median follow-up of 35 months (range, 0.5-132 mo).[ncbi.nlm.nih.gov]

    Missing: Abnormal Corticomedullary Differentiation
  • Senior-Løken Syndrome

    […] diagnosis of these varieties of hereditary tapeto-retinal degeneration.[ncbi.nlm.nih.gov] Absence of renal corticomedullary differentiation Short proximal phalanx of finger Vascular ring Aplasia of the middle phalanx of the hand Pyelonephritis Frontal upsweep[mendelian.co] Mutations in nine genes are linked to retinal degeneration and mutated NPHP1 to NPHP13 genes result in nephronophthisis.[symptoma.com]

    Missing: Gastric Adenocarcinoma
  • Meningeal Carcinomatosis

    Leptomeningeal involvement is usually reported as a secondary event in advanced, already diagnosed, gastric adenocarcinoma.[ncbi.nlm.nih.gov] Loss of vision in three patients secondary to retinal photoreceptor degeneration aa a remote effect of cancer was reported by Sawyer and associated A combined mechanism may[healio.com] However, gastric adenocarcinoma has been rarely reported with leptomeningeal carcinomatosis.[ncbi.nlm.nih.gov]

    Missing: Abnormal Corticomedullary Differentiation
  • Nephronophthisis 1

    Mutations in AHI1, which encodes a cilium-localized protein, have been shown to cause a form of Joubert syndrome that is highly penetrant for retinal degeneration.[ncbi.nlm.nih.gov] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com]

    Missing: Gastric Adenocarcinoma
  • Nephronophthisis 3

    […] coworkers2 was called by them: "a retinal dystrophy undistlnguishable from Leber's tapeto retinal degeneration."[healio.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com]

    Missing: Gastric Adenocarcinoma
  • Nephronophthisis 12

    Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov] degeneration.[doi.org]

    Missing: Gastric Adenocarcinoma
  • Nephronophthisis 9

    Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov] degeneration.[oadoi.org]

    Missing: Gastric Adenocarcinoma
  • Nephronophthisis 2

    Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov] Extrarenal manifestations occur in 10–15% including retinal degeneration, cerebellar vermis hypoplasia and liver fibrosis, requiring referral to other specialists.[oxfordmedicine.com]

    Missing: Gastric Adenocarcinoma
  • Retinitis Pigmentosa 41

    PMID 30061254 CD133 Expression as a Helicobacter pylori -independent Biomarker of Gastric Cancer Progression. Howard R, et al . Anticancer Res, 2018 Aug.[ncbi.nlm.nih.gov] PROM1 is also implicated in other diseases associated with retinal degeneration ( OMIM:604365 ).[flybase.org] Synonyms RP 41 Retinal degeneration, autosomal recessive, prominin-related Overview No overview is available at this time. Please check back for future updates.[rarediseases.org]

    Missing: Abnormal Corticomedullary Differentiation

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