Villous atrophy

Symptom Information:

Symptom ID: HPO:0011473
Synonyms:
Atrophy of small intestinal villi [HPO:0011473]
BIOPSY SHOWS VILLOUS ATROPHY [HPO:0011473]
DUODENAL VILLOUS ATROPHY [HPO:0011473]
SMALL INTESTINE BIOPSY SHOWS VILLOUS ATROPHY [HPO:0011473]
VARIABLE DEGREE OF VILLOUS ATROPHY [HPO:0011473]
Biopsy shows villous atrophy [OMIM:Biopsy shows villous atrophy]
Duodenal villous atrophy [OMIM:Duodenal villous atrophy]
Small intestine biopsy shows villous atrophy [OMIM:Small intestine biopsy shows villous atrophy]
Variable degree of villous atrophy [OMIM:Variable degree of villous atrophy]
Villous atrophy [OMIM:Villous atrophy]
Quality:
Cross references:
OMIM: "Biopsy shows villous atrophy" [OMIM:Biopsy shows villous atrophy]
OMIM: "Duodenal villous atrophy" [OMIM:Duodenal villous atrophy]
OMIM: "Small intestine biopsy shows villous atrophy" [OMIM:Small intestine biopsy shows villous atrophy]
OMIM: "Variable degree of villous atrophy" [OMIM:Variable degree of villous atrophy]
OMIM: "Villous atrophy" [OMIM:Villous atrophy]
Is a (Direct Parents):
HPO         Abnormality of small intestinal villus morphology
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:
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)