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205720009: Fragile X chromosome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
315486012 Fragile X chromosome en Synonym Active Only initial character case insensitive SNOMED CT core module
591126013 Fragile X chromosome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fragile X chromosome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
Fragile X chromosome Is a Fragile X syndrome false Inferred relationship Existential restriction modifier
Fragile X chromosome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Fragile X chromosome Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Occurrence Congenital false Inferred relationship Existential restriction modifier
Fragile X chromosome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Fragile X chromosome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Fragile X chromosome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Fragile X chromosome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Fragile X chromosome Associated morphology Chromosomal morphology true Inferred relationship Existential restriction modifier 2
Fragile X chromosome Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
FRAXA Is a True Fragile X chromosome Inferred relationship Existential restriction modifier
FRAXE Is a True Fragile X chromosome Inferred relationship Existential restriction modifier
FRAXF syndrome Is a True Fragile X chromosome Inferred relationship Existential restriction modifier
FRAXE intellectual disability syndrome Is a True Fragile X chromosome Inferred relationship Existential restriction modifier
Fragile X chromosome screening test Has focus True Fragile X chromosome Inferred relationship Existential restriction modifier 3
Fragile X syndrome Is a True Fragile X chromosome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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