Other specified congenital anomalies of kidney
751.22
Congenital Anomalies
Both
750-751.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| Q60 | ICD10CM | Renal agenesis and other reduction defects of kidney | MGI |
| Q60.0 | ICD10CM | Renal agenesis, unilateral | MGI |
| Q60.1 | ICD10CM | Renal agenesis, bilateral | MGI |
| Q60.2 | ICD10CM | Renal agenesis, unspecified | MGI |
| Q60.3 | ICD10CM | Renal hypoplasia, unilateral | MGI |
| Q60.4 | ICD10CM | Renal hypoplasia, bilateral | MGI |
| Q60.5 | ICD10CM | Renal hypoplasia, unspecified | MGI |
| Q60.6 | ICD10CM | Potter's syndrome | MGI |
| Q63 | ICD10CM | Other congenital malformations of kidney | MGI |
| Q63.0 | ICD10CM | Accessory kidney | MGI |
| Q63.1 | ICD10CM | Lobulated, fused and horseshoe kidney | MGI |
| Q63.2 | ICD10CM | Ectopic kidney | MGI |
| Q63.3 | ICD10CM | Hyperplastic and giant kidney | MGI |
| Q63.8 | ICD10CM | Other specified congenital malformations of kidney | MGI |
| Q63.9 | ICD10CM | Congenital malformation of kidney, unspecified | MGI |
| 753.0 | ICD9CM | Renal agenesis and dysgenesis | MGI |
| 753.3 | ICD9CM | Other specified anomalies of kidney | MGI |
| Q60.0 | ICD10 | Q60.0 Renal agenesis, unilateral | UKB |
| Q60.2 | ICD10 | Q60.2 Renal agenesis, unspecified | UKB |
| Q60.3 | ICD10 | Q60.3 Renal hypoplasia, unilateral | UKB |
| Q60.5 | ICD10 | Q60.5 Renal hypoplasia, unspecified | UKB |
| Q60.6 | ICD10 | Q60.6 Potter's syndrome | UKB |
| Q63.0 | ICD10 | Q63.0 Accessory kidney | UKB |
| Q63.1 | ICD10 | Q63.1 Lobulated, fused and horseshoe kidney | UKB |
| Q63.2 | ICD10 | Q63.2 Ectopic kidney | UKB |
| Q63.8 | ICD10 | Q63.8 Other specified congenital malformations of kidney | UKB |
| Q63.9 | ICD10 | Q63.9 Congenital malformation of kidney, unspecified | UKB |
| 753.0 | ICD9 | 7530 Renal agenesis and dysgenesis | UKB |
| 753.3 | ICD9 | 7533 Other specified anomalies of kidney | UKB |
This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.