| General Information | |||
|---|---|---|---|
| Term | Dent disease | ID (Ontology) | DOID:0050699 (Human Disease) |
| Definition | A renal tubular transport disease that is characterized by tubular proteinuria, hypercalciuria, calcium nephrolithiasis, nephrocalcinosis and chronic kidney failure. | ||
| Also Known As | "Dent's disease" ; "X-linked hypercalciuric nephrocalcinosis" | ||
| 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
|
|||
|
||||||
X-linked monogenic disease |__X-linked recessive disease_______ kidney disease | |__renal tubular transport disease__| Dent disease 4 rec. |__Dent disease 1 2 rec. |__Dent disease 2 1 rec. |__low molecular weight proteinuria with hypercalciuric nephrocalcinosis 3 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
X-linked recessive disease renal tubular transport disease |
||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:13105 MESH:D057973 MIM:300009 MIM:300555 NCI:C123260 ORDO:1652 SNOMEDCT_US_2023_03_01:444645005 UMLS_CUI:C0878681 |
|||