1216942009: Cerebral ventriculomegaly, cystic kidney disease (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

5033755019 Congenital nephrosis, cerebral ventriculomegaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5033756018 VMCKD - ventriculomegaly with cystic kidney disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5033757010 Cerebral ventriculomegaly, cystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5033758017 Cerebral ventriculomegaly, cystic kidney disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5033762011 A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, gray matter heterotopias and cardiac malformations among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5033763018 A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, grey matter heterotopias and cardiac malformations among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Congenital cerebral ventriculomegaly (disorder)	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Hereditary disorder of nervous system	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Hereditary nephropathy (disorder)	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Multiple congenital cysts of kidney	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Cerebral ventriculomegaly, cystic kidney disease	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Cerebral ventriculomegaly, cystic kidney disease	localisation d'une constatation (attribut)	structure d'un rein	true	Inferred relationship	Some	1
Cerebral ventriculomegaly, cystic kidney disease	morphologie associée (attribut)	Polycystic change	true	Inferred relationship	Some	1
Cerebral ventriculomegaly, cystic kidney disease	survenue (attribut)	congénital	true	Inferred relationship	Some	2
Cerebral ventriculomegaly, cystic kidney disease	localisation d'une constatation (attribut)	Entire ventricle of brain	true	Inferred relationship	Some	2
Cerebral ventriculomegaly, cystic kidney disease	morphologie associée (attribut)	Enlargement (morphologic abnormality)	true	Inferred relationship	Some	2
Cerebral ventriculomegaly, cystic kidney disease	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
5033755019	Congenital nephrosis, cerebral ventriculomegaly syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5033756018	VMCKD - ventriculomegaly with cystic kidney disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5033757010	Cerebral ventriculomegaly, cystic kidney disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5033758017	Cerebral ventriculomegaly, cystic kidney disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5033762011	A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, gray matter heterotopias and cardiac malformations among others.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5033763018	A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, grey matter heterotopias and cardiac malformations among others.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core