MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandintestinal disease (MONDO:0005020)
..Starting node
..expandintractable diarrhea of infancy ()

       Child Nodes:
........expandautoimmune enteropathy type 2 ()
........expandautoimmune enteropathy type 3 ()
........expandchronic diarrhea with villous atrophy ()  LSDB  L: 00164;
........expandcombined immunodeficiency due to LRBA deficiency ()
........expandcongenital diarrhea 5 with tufting enteropathy ()
........expandcongenital diarrhea 7 with exudative enteropathy ()
........expandimmune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome ()
........expandintractable diarrhea-choanal atresia-eye anomalies syndrome ()
........expandmicrovillus inclusion disease ()
........expandsyndromic multisystem autoimmune disease due to Itch deficiency ()
........expandtricho-hepato-enteric syndrome ()



 Sister Nodes: 
..expandAeromonas hydrophila intestinal disease ()
..expandangiodysplasia of intestine ()
..expandaplasia cutis congenita-intestinal lymphangiectasia syndrome ()
..expandbowel dysfunction ()
..expandchronic atrial and intestinal dysrhythmia ()
..expandchronic enteropathy associated with SLCO2A1 gene ()
..expandchronic intestinal failure ()
..expandchronic intestinal vascular insufficiency ()
..expandcongenital enteropathy involving intestinal mucosa development ()
..expandcongenital intestinal disease due to an enzymatic defect ()
..expandcongenital intestinal transport defect ()
..expandcryptogenic multifocal ulcerous stenosing enteritis ()
..expandcytosolic phospholipase-A2 alpha deficiency associated bleeding disorder ()
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..expandintestinal lymphangiectasia (disease) ()
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..expandintestinal neoplasm ()
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..expandintestinal perforation ()
..expandintractable diarrhea of infancy ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19126
Name:intractable diarrhea of infancy
Definition:Intractable diarrhoea of infancy (IDI) is a heterogeneous syndrome that includes several diseases with different aetiologies. Provisional classification of IDI, according to villous atrophy and based on immunohistological criteria, distinguishes two clearly different groups of IDI: 1) Immune-mediated: characterised by a mononuclear cell infiltration of the lamina propria and considered as being related to T cell activation. 2) The second histological pattern includes early onset severe intractable diarrhoea histologically characterised by villous atrophy with low or without mononuclear cell infiltration of the lamina propria but specific histological abnormalities involving the epithelium.
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Synonyms:IDI
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