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Intestinal epithelial dysplasia
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary nonpolyposis colon cancer
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Synonym(s):
- Congenital familial intractable diarrhea with epithelial or epithelium abnormalities
- IED
- Tufting enteropathy
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
EPCAM P16422185535
No signs/symptoms info available.