| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| NPHP3-related Meckel-like syndrome |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Hepatic fibrosis, renal cyst, intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Counseling for congenital polycystic kidney disease (procedure) |
a pour objet (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
2 |
| Cerebral ventriculomegaly, cystic kidney disease |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Polycystic kidney disease, adult type |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Polycystic kidney disease, infantile type |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Medullary cystic disease of the kidney |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Microcystic renal disease (disorder) |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Simple renal cyst |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| FH: Polycystic kidney |
constatation associée (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
1 |
| Solitary multilocular renal cyst |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| FH: Polycystic kidney |
constatation associée (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
1 |
| FH: Polycystic kidney |
constatation associée (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
1 |
| Other specified congenital cystic kidney disease |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| [X]Other cystic kidney diseases |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| ectasie canaliculaire précalicielle |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome (disorder) |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Fibrocystic kidney disease |
est un(e) (attribut) |
False |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Renal hepatic pancreatic dysplasia (disorder) |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|
| Autosomal dominant polycystic kidney disease (disorder) |
est un(e) (attribut) |
True |
Multiple congenital cysts of kidney |
Inferred relationship |
Some |
|