Cytoscape Web
Click node...

Syndromic diarrhea
2 OMIM references -
2 associated genes
9 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical Rett syndrome
Burkitt lymphoma
Cowden syndrome
Heritable pulmonary arterial hypertension
Precursor T-cell acute lymphoblastic leukemia
Proteus syndrome
Pseudohypoaldosteronism type 2E
Split hand-split foot malformation
West syndrome
Synonym(s):
- Phenotypic diarrhea
- SD/THE
- Syndromatic diarrhea
- Syndromic diarrhea/Tricho-hepato-enteric syndrome
- Tricho-hepato-enteric syndrome
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
SKIV2L Q15477600478
TTC37 Q6PGP7614589
No signs/symptoms info available.