Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bilateral renal dysplasia |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Unilateral renal dysplasi |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Congenital renal dysplasia |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
nyredysplasi, ikke nærmere specificeret |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
[EDTA] Congenital renal dysplasia with or without urinary tract malformation associated with renal failure |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Unilateral renal dysplasi |
Associated finding |
False |
Renal dysplasia |
Inferred relationship |
Some |
1 |
Unilateral renal dysplasi |
Associated finding |
False |
Renal dysplasia |
Inferred relationship |
Some |
1 |
Saldino-Mainzer dysplasia |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
Renal dysplasia co-occurrent with megalocystis and sirenomelia |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Ulbright-Hodes syndrome is characterized by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a Potter-like facies. The syndrome has been described in three infants (one pair of siblings and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive. |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
Primary renal dysplasia (disorder) |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
Secondary renal dysplasia (disorder) |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
This syndrome is characterized by intrauterine growth retardation, renal dysgenesis and a unilobed or absent thymus. |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
Agenesis of right kidney co-occurrent with congenital dysplasia of left kidney (disorder) |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Agenesis of left kidney co-occurrent with congenital dysplasia of right kidney (disorder) |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Dysplasia of left kidney |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
Dysplasia of right kidney |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
An extremely rare developmental defect during embryogenesis malformation syndrome with congenital muscular torticollis associated with skin anomalies (such as multiple keloids, pigmented nevi, epithelioma), urogenital malformations (including cryptorchidism and hypospadias) and renal dysplasia (for example chronic pyelonephritis, renal atrophy). Additional reported features include varicose veins, intellectual disability and musculoskeletal anomalies. |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|
A rare congenital anomaly of the kidney and urinary tract (CAKUT) in which one or both kidneys (unilateral or bilateral MCDK respectively) are large, distended by multiple cysts, and non-functional. Unilateral MCDK is typically asymptomatic if the other kidney is fully functional but may occasionally present with abdominal obstructive signs when the cysts become too large. Bilateral MCDK is considered a lethal entity and neonates present with features of the Potter sequence, severe pulmonary hypoplasia and severe renal failure, and generally die shortly after birth. |
Is a |
False |
Renal dysplasia |
Inferred relationship |
Some |
|
Cystic dysplasia of kidney (disorder) |
Is a |
True |
Renal dysplasia |
Inferred relationship |
Some |
|