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723332005: Isodicentric chromosome 15 syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3424112014 Isodicentric chromosome 15 syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424113016 Isodicentric chromosome 15 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424114010 Duplication/inversion 15q11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424115011 Isodicentric 15 chromosome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424116012 Inverted duplication 15 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424117015 Non-distal tetrasomy 15q en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424118013 A chromosomal disorder with distinctive clinical findings characterized by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behavior. Facial dysmorphism is absent or subtle and major malformations are rare. The syndrome is usually sporadic and not inherited and results from an abnormal extra chromosome in each cell containing mirror-image segments of genetic material. The isodicentric chromosome is made up of two extra copies of a segment of genetic material from chromosome 15, which is attached end-to-end. Typically this copied genetic material includes a region of the chromosome called 15q11-q13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424119017 A chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour. Facial dysmorphism is absent or subtle and major malformations are rare. The syndrome is usually sporadic and not inherited and results from an abnormal extra chromosome in each cell containing mirror-image segments of genetic material. The isodicentric chromosome is made up of two extra copies of a segment of genetic material from chromosome 15, which is attached end-to-end. Typically this copied genetic material includes a region of the chromosome called 15q11-q13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
11392621000172113 tétrasomie non distale 15q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11392631000172111 syndrome du chromosome 15 isodicentrique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11392641000172116 syndrome de duplication inversée du chromosome 15 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5125701000172116 IDIC-15 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
5125711000172118 SMC15 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
5125721000172111 niet-distale tetrasomie 15q nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5125731000172114 inverted duplication 15 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5125741000172119 'supernumerary marker 15'-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5125751000172117 isodicentrisch chromosoom 15 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5125761000172115 partiële tetrasomie 15 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isodicentric chromosome 15 syndrome (disorder) Is a Anomaly of chromosome pair 15 true Inferred relationship Some
Isodicentric chromosome 15 syndrome (disorder) Is a Pervasive developmental disorder (disorder) true Inferred relationship Some
Isodicentric chromosome 15 syndrome (disorder) Is a retard mental false Inferred relationship Some
Isodicentric chromosome 15 syndrome (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Some 1
Isodicentric chromosome 15 syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Isodicentric chromosome 15 syndrome (disorder) Finding site Chromosome pair 15 true Inferred relationship Some 1
Isodicentric chromosome 15 syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Isodicentric chromosome 15 syndrome (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Isodicentric chromosome 15 syndrome (disorder) Is a Congenital malformation true Inferred relationship Some
Isodicentric chromosome 15 syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Isodicentric chromosome 15 syndrome (disorder) Associated morphology Tetrasomy true Inferred relationship Some 1
Isodicentric chromosome 15 syndrome (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 2
Isodicentric chromosome 15 syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 2
Isodicentric chromosome 15 syndrome (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
Isodicentric chromosome 15 syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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