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718556007: Cranio-cerebello-cardiac dysplasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312750013 Craniocerebellocardiac dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312751012 Ritscher Schinzel syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312752017 3C syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3312754016 Cranio-cerebello-cardiac dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312755015 Cranio-cerebello-cardiac dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401760011 Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterized by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401761010 Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterised by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312750013 Craniocerebellocardiac dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3312750013 Craniocerebellocardiac dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312751012 Ritscher Schinzel syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312752017 3C syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3312754016 Cranio-cerebello-cardiac dysplasia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3312754016 Cranio-cerebello-cardiac dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312755015 Cranio-cerebello-cardiac dysplasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3312755015 Cranio-cerebello-cardiac dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312753010 A rare multiple congenital anomalies syndrome with characteristics of craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies. To date less than 50 cases have been described. The exact cause is still unknown but mutations in KIAA0196 (8q24.13; coding for strumpellin) have been identified. Sporadic and familial cases have been reported. Transmission is autosomal recessive. Phenotypic variability exists between siblings. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401760011 Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterized by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401761010 Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterised by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3395371001000115 3C-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5479361000241112 dysplasie cranio-cérébello-cardiaque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5479361000241112 dysplasie cranio-cérébello-cardiaque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395371001000115 3C-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
3C syndrome Is a Congenital heart disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
3C syndrome Is a Congenital anomaly of brain true Inferred relationship Existential restriction modifier (core metadata concept)
3C syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
3C syndrome Is a Congenital abnormality of skull and face bones (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
3C syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
3C syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
3C syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
3C syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
3C syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 7
3C syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 7
3C syndrome Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 5
3C syndrome Finding site Bone structure of head false Inferred relationship Existential restriction modifier (core metadata concept) 7
3C syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 6
3C syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
3C syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
3C syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
3C syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
3C syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
3C syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
3C syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
3C syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
3C syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
3C syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
3C syndrome Finding site Heart structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
3C syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
3C syndrome Finding site Bone structure of head true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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