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Congenital chloride diarrhea
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C536210
Gene symbol UniProt reference OMIM reference
SLC26A3 P40879126650
No signs/symptoms info available.