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34 Possible Causes for Congenital Secretory Sodium Diarrhea

  • Steatorrhea

    […] microvillous atrophy Congenital secretory diarrhea Congenital secretory diarrhea, chloride type Congenital secretory diarrhea, sodium type Drug induced malabsorption Drug-induced[icd9data.com] […] acid malabsorption syndrome type I Bile acid malabsorption syndrome type II Bile acid malabsorption syndrome type III Chemically-induced malabsorption Chronic steatorrhea Congenital[icd9data.com]

  • Protein Losing Enteropathy

    […] microvillous atrophy Congenital secretory diarrhea Congenital secretory diarrhea, chloride type Congenital secretory diarrhea, sodium type Drug induced malabsorption Drug-induced[icd9data.com] […] acid malabsorption syndrome type I Bile acid malabsorption syndrome type II Bile acid malabsorption syndrome type III Chemically-induced malabsorption Chronic steatorrhea Congenital[icd9data.com]

  • Allan-Herndon-Dudley Syndrome

    Syndrome congenital hypothyroidism congenital secretory sodium diarrhea 3 Congenital Woolly Hair Contiguous Abcd1/Dxs1375e Deletion Syndrome Copper Deficiency, Familial Benign[rgd.mcw.edu] Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation Congenital Hypoplastic Anemia with Multiple Congenital Anomalies/Mental Retardation[rgd.mcw.edu] URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE Congenital[rgd.mcw.edu]

  • VIPoma

    In children, rarely inherited electrolyte transport defects, like congenital chloride diarrhea and congenital sodium diarrhea may cause secretory diarrhea.[statpearls.com]

  • Congenital Chloride Diarrhea

    […] microvillous atrophy Congenital secretory diarrhea Congenital secretory diarrhea, chloride type Congenital secretory diarrhea, sodium type Drug induced malabsorption Drug-induced[icd9data.com] […] acid malabsorption syndrome type I Bile acid malabsorption syndrome type II Bile acid malabsorption syndrome type III Chemically-induced malabsorption Chronic steatorrhea Congenital[icd9data.com]

  • Congenital Optic Disc Coloboma

    Congenital sodium diarrhea is a rare and life-threatening disorder characterized by a severe, secretory diarrhea containing high concentrations of sodium, leading to hyponatremia[ncbi.nlm.nih.gov]

  • Congenitally Short Costocoracoid Ligament

    Congenital radio-ulnar synostosis Congenital secretory diarrhea, chloride type Congenital secretory diarrhea, sodium type Congenital sensory neuropathy with selective loss[diseaseinfosearch.org] […] nongoitrous hypothyroidism Congenital Nonhemolytic Jaundice Congenital patellar dislocation (CPD) Congenital phenobarbital exposure Congenital Porphyria Congenital Pseudoarthrosis[diseaseinfosearch.org] Congenital myopathy Congenital myopathy with caps Congenital myopathy with fiber type disproportion Congenital Myotonic Dystrophy Congenital Nephrotic Syndrome Finnish Type Congenital[diseaseinfosearch.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    3, secretory sodium, congenital, syndromic 1 Diarrhea 4, malabsorptive, congenital (NEUROG3) 1 Diarrhea 5, with tufting enteropathy, congenital (EPCAM) 1 DiGeorge Syndrome[viafet.com] Syndrome (EGR2, MPZ, PMP22) 3 Dent disease (CLCN5, OCRL) 2 Dentin Dysplasia (DSPP, SMOC2) 2 Denys-Drash Syndrome (WT1) 1 Diabetes insipidus, nephrogenic (AQP2, AVPR2) 2 Diarrhea[viafet.com]

  • Syndromic Diarrhea

    MalaCards based summary : Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies, also known as diarrhea 3, secretory sodium, congenital, syndromic[malacards.org] UniProtKB/Swiss-Prot : 76 Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies: A disease characterized by life-threatening secretory diarrhea[malacards.org] An important gene associated with Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies is SPINT2 (Serine Peptidase Inhibitor, Kunitz Type 2[malacards.org]

  • Palmoplantar Keratoderma-Spastic Paralysis Syndrome

    […] amaurosis 3 Juvenile amyotrophic lateral sclerosis 5 GHR GeneReviews OMIM SPINT2 Congenital secretory sodium diarrhea 3 GeneReviews OMIM SRD5A2 Pseudovaginal perineoscrotal[genepeeks.com] Niemann-Pick disease, type B GHR GeneReviews OMIM SNAP29 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome GHR GeneReviews OMIM SPATA7 Leber congenital[genepeeks.com]

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