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Congenital enteropathy due to enteropeptidase deficiency
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary chronic pancreatitis
Tropical pancreatitis
Familial expansile osteolysis
Osteopetrosis - hypogammaglobulinemia
Synonym(s):
- Congenital enterokinase deficiency
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
TMPRSS15 P98073606635
No signs/symptoms info available.