Disease #00088 (DIAR1 (diarrhea, type 1, chloride, secretory, congenital (Finnish type, DIAR-1)), OMIM:214700)
Official abbreviation |
DIAR1 |
Name |
diarrhea, type 1, chloride, secretory, congenital (Finnish type, DIAR-1) |
OMIM ID |
214700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
69 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
SLC26A3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-11-20 12:45:29 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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