Glycosuria, Renal
Disease ID: disease_node_3544
Connections displayed (default: 10).
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| Dbxref | GARD:7548, MESH:D006030, MIM:233100, ORDO:69076, SNOMEDCT_US_2023_03_01:226309007, UMLS_CUI:C3245525 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050737, DOID_9432 |
| Data Source | DOID, MESH |
| Synonyms | FRG, SGLT2 deficiency, familial renal glycosuria, hereditary renal glycosuria |
| Mesh Id | D006030 |
| Mesh Label | Glycosuria, Renal |
| Mesh Subclassof | D015499, D006029 |
| Doid Label | familial renal glucosuria |
| Doid Description | A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_3544 |
| Doid Id | DOID_0070613 |
| Label | Glycosuria, Renal |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Renal Glycosuria(ID:disease_node_13649) (Disease)