65071000119106: Family history of fragile X syndrome (situation)

SNOMED CT Concept\Situation with explicit context (situation)\...

\Finding with explicit context (situation)\Family history of clinical finding\Family history of disorder\...

\Family history of hereditary disease (situation)\Family history of fragile X syndrome (situation)

\Family history of development disorder\Family history of multiple congenital anomalies (situation)\Family history of fragile X syndrome (situation)
\Family history of development disorder\Family history of intellectual disability\Family history of fragile X syndrome (situation)

\Family history of congenital disease (situation)\Family history of multiple congenital anomalies (situation)\Family history of fragile X syndrome (situation)
\Family history of congenital disease (situation)\Family history of chromosomal anomaly (situation)\Family history of fragile X syndrome (situation)

\Family history with explicit context (situation)\Family history of clinical finding\Family history of disorder\...

\Family history of hereditary disease (situation)\Family history of fragile X syndrome (situation)

\Family history of development disorder\Family history of multiple congenital anomalies (situation)\Family history of fragile X syndrome (situation)
\Family history of development disorder\Family history of intellectual disability\Family history of fragile X syndrome (situation)

\Family history of congenital disease (situation)\Family history of multiple congenital anomalies (situation)\Family history of fragile X syndrome (situation)
\Family history of congenital disease (situation)\Family history of chromosomal anomaly (situation)\Family history of fragile X syndrome (situation)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3078051011 Family history of fragile X syndrome (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3078055019 Family history of fragile X syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3790191000052116 hereditet för fragil X-syndromet sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Family history of fragile X syndrome (situation)	Is a	Family history of chromosomal anomaly (situation)	true	Inferred relationship	Some
Family history of fragile X syndrome (situation)	Associated finding	Fragile X syndrome	true	Inferred relationship	Some	1
Family history of fragile X syndrome (situation)	Subject relationship context (attribute)	person inom patientens familj	false	Inferred relationship	Some	1
Family history of fragile X syndrome (situation)	Temporal context (attribute)	Current or past (actual) (qualifier value)	true	Inferred relationship	Some	1
Family history of fragile X syndrome (situation)	Finding context (attribute)	Known present (qualifier value)	true	Inferred relationship	Some	1
Family history of fragile X syndrome (situation)	Is a	Family history of multiple congenital anomalies (situation)	true	Inferred relationship	Some
Family history of fragile X syndrome (situation)	Is a	Family history of intellectual disability	true	Inferred relationship	Some
Family history of fragile X syndrome (situation)	Is a	Family history of hereditary disease (situation)	true	Inferred relationship	Some
Family history of fragile X syndrome (situation)	Subject relationship context (attribute)	Person in the family (person)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets