Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Medullary cystic disease (disorder) |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Medullary sponge kidney |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fibrocystic kidney disease (disorder) |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
polykystose rénale autosomique dominante |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Polycystic kidney disease, infantile type |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Microcystic renal disease |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Simple renal cyst |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Solitary multilocular renal cyst |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other specified congenital cystic kidney disease |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
[X]Other cystic kidney diseases |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
FH: Polycystic kidney |
Associated finding |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
FH: Polycystic kidney |
Associated finding |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
FH: Polycystic kidney |
Associated finding |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multinodular goiter, cystic kidney, polydactyly syndrome |
Is a |
False |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome (disorder) |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Renal hepatic pancreatic dysplasia (disorder) |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal dominant polycystic kidney disease |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Nephrocystin 3-related Meckel-like syndrome (disorder) |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare syndromic intellectual disability characterised by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnoea. There have been no further descriptions in the literature since 1987. |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Counselling for congenital polycystic kidney disease |
Has focus |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cerebral ventriculomegaly, cystic kidney disease |
Is a |
True |
Congenital cystic kidney disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|