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66661000119103: Carrier of fragile X chromosome (finding)


Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3433701015 Carrier of fragile X chromosome (finding) en Fully specified name Active Initial character case insensitive SNOMED CT core
3433702010 Carrier of fragile X chromosome en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of fragile X chromosome Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Carrier of fragile X chromosome Has interpretation Detected true Inferred relationship Some 2
Carrier of fragile X chromosome Associated morphology Chromosomal morphology true Inferred relationship Some 3
Carrier of fragile X chromosome Interprets Fragile X chromosome screening test true Inferred relationship Some 2
Carrier of fragile X chromosome Finding site Sex chromosome X true Inferred relationship Some 3
Carrier of fragile X chromosome Is a Gastrointestinal hormone level - finding true Inferred relationship Some
Carrier of fragile X chromosome Associated morphology Congenital anomaly false Inferred relationship Some
Carrier of fragile X chromosome Is a Genetic disorder carrier true Inferred relationship Some
Carrier of fragile X chromosome Is a Presence of drug - finding false Inferred relationship Some
Carrier of fragile X chromosome Is a Hormone level - finding false Inferred relationship Some
Carrier of fragile X chromosome Interprets General clinical state true Inferred relationship Some 1
Carrier of fragile X chromosome Has interpretation Present false Inferred relationship Some 3
Carrier of fragile X chromosome Interprets Fragile X chromosome screening test false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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