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renal agenesis
Summary
- Synonym
-
- hereditary renal aplasia
- hereditary urogenital adysplasia
- renal adysplasia
- renal aplasia
- Definition
- A renal disease that is characterized by the failure of one or both kidneys to develop.
- Super Class
- kidney disease
External Links
- Disease Ontology
- DOID:14766
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2218 | FKTN | fukutin | |
| 2674 | GFRA1 | GDNF family receptor alpha 1 | |
| 2719 | GPC3 | glypican 3 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 9091 | PIGQ | phosphatidylinositol glycan anchor biosynthesis class Q | |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 | |
| 10585 | POMT1 | protein O-mannosyltransferase 1 | |
| 23556 | PIGN | phosphatidylinositol glycan anchor biosynthesis class N | |
| 29954 | POMT2 | protein O-mannosyltransferase 2 | |
| 51227 | PIGP | phosphatidylinositol glycan anchor biosynthesis class P |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002089 | Pulmonary hypoplasia |
| HP:0000175 | Cleft palate |
| HP:0010497 | Sirenomelia |
| HP:0000457 | Depressed nasal ridge |
| HP:0100335 | Non-midline cleft of the upper lip |
| HP:0001563 | Fetal polyuria |
| HP:0000316 | Hypertelorism |
| HP:0002575 | Tracheoesophageal fistula |
