Villous atrophy
Symptom Information:
Symptom ID: | HPO:0011473 | ||||||||||
Synonyms: |
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Quality: | |||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the intestine(HPO:0002242) Abnormality of the small intestine(HPO:0002244) Abnormality of small intestinal villus morphology(HPO:0011472) Villous atrophy(HPO:0011473) MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
ALG3-CDG | (Orphanet:79321) |
IMMUNODEFICIENCY 31C | (OMIM:614162) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunodeficiency by defective expression of HLA class 2 | (Orphanet:572) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Intestinal epithelial dysplasia | (Orphanet:92050) |
MPI-CDG | (Orphanet:79319) |
Microvillous inclusion disease | (Orphanet:2290) |
Neonatal inflammatory skin and bowel disease | (Orphanet:294023) |
Netherton syndrome | (Orphanet:634) |
Obesity due to prohormone convertase I deficiency | (Orphanet:71528) |
Syndromic diarrhea | (Orphanet:84064) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |