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764711007: Xq12-q13.3 duplication syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3654884010 Xq12-q13.3 duplication syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3654885011 Xq12-q13.3 duplication syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xq12-q13.3 duplication syndrome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
Xq12-q13.3 duplication syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Xq12-q13.3 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
Xq12-q13.3 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Xq12-q13.3 duplication syndrome Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Xq12-q13.3 duplication syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
Xq12-q13.3 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Xq12-q13.3 duplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Xq12-q13.3 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
Xq12-q13.3 duplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Xq12-q13.3 duplication syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Xq12-q13.3 duplication syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Xq12-q13.3 duplication syndrome Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Xq12-q13.3 duplication syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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