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763275001: Distal trisomy 6q (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3638358012 Distal trisomy 6q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3638359016 Distal trisomy 6q (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3638360014 Distal duplication 6q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403983012 Distal trisomy 6q is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6, with highly variable phenotype, typically characterized by growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short, webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity, and seizures, are other features that have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403984018 Distal trisomy 6q is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6, with highly variable phenotype, typically characterised by growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short, webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity, and seizures, are other features that have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3638358012 Distal trisomy 6q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3638359016 Distal trisomy 6q (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3638360014 Distal duplication 6q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3638361013 A rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6. The disorder has a highly variable phenotype with typical characteristics of growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity and seizures are other features that have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403983012 Distal trisomy 6q is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6, with highly variable phenotype, typically characterized by growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short, webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity, and seizures, are other features that have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403984018 Distal trisomy 6q is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6, with highly variable phenotype, typically characterised by growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short, webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity, and seizures, are other features that have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437371001000113 Trisomie 6q, distale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929061000172119 duplication distale 6q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
954091000172112 trisomie distale 6q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929061000172119 duplication distale 6q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
954091000172112 trisomie distale 6q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437371001000113 Trisomie 6q, distale 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
Distal trisomy 6q Is a 6q partial trisomy syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Distal trisomy 6q Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 6q Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 6q Finding site Chromosome pair 6 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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