Gastroenterology · Gastroenterology / Pediatric GI disease
Congenital chloride diarrhea syndrome
also: Congenital chloridorrhea
Chloride-rich watery diarrhea from birth.
- Specialty
- Gastroenterology
- Subspecialty
- Gastroenterology / Pediatric GI disease
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, neonatal onset
- Gene(s) involved
- SLC26A3
- Alternative names & eponyms
- Congenital chloridorrhea
Etiology & mechanism
Defective ileal and colonic Cl-/HCO3- exchange.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Congenital chloride diarrhea syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Bartter syndrome
metabolic alkalosis, polyhydramnios
1 shared
Burnett syndrome
metabolic alkalosis
1 shared
Cyclic vomiting syndrome
dehydration
1 shared
EAST syndrome
metabolic alkalosis
1 shared
Fanconi syndrome
dehydration
1 shared
Kagami–Ogata syndrome
polyhydramnios
1 shared
Liddle syndrome
metabolic alkalosis
1 shared
Short bowel syndrome
dehydration
1 shared
Toxic epidermal necrolysis
dehydration
1 shared
Transient neonatal diabetes syndrome
dehydration
Shares genes with
None.
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