| General Information | |||
|---|---|---|---|
| Term | congenital secretory sodium diarrhea 8 | ID (Ontology) | DOID:0060777 (Human Disease) |
| Definition | A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SLC9A3 gene on chromosome 5p15. | ||
| Also Known As | "DIAR8" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
||||||
autosomal genetic disease |__autosomal recessive disease__ diarrhea | |__secretory diarrhea___________| disease | |__physical disorder____________| congenital secretory sodium diarrhea 8 1 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
secretory diarrhea autosomal recessive disease physical disorder |
||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:P78.3 MIM:616868 ORDO:103908 |
|||