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63931000119106: myotone dystrofie type 1 in familieanamnese (situatie)


Status: current, 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
3467660017 Family history of Steinert myotonic dystrophy (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3467661018 Family history of Steinert myotonic dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3467662013 Family history of myotonic muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160631000146112 myotone dystrofie type 1 in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5160641000146116 ziekte van Steinert in familieanamnese nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5160651000146118 myotone dystrofie type 1 in familieanamnese (situatie) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5160661000146115 dystrophia myotonica type 1 in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5160671000146114 myotonia dystrophica type 1 in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of Steinert myotonic dystrophy (situation) Is a FH: Muscular dystrophy true Inferred relationship Some
Family history of Steinert myotonic dystrophy (situation) Is a Family history of multiple congenital anomalies (situation) false Inferred relationship Some
Family history of Steinert myotonic dystrophy (situation) Associated finding Steinert myotonic dystrophy syndrome true Inferred relationship Some 1
Family history of Steinert myotonic dystrophy (situation) Finding context (attribute) Known present (qualifier value) true Inferred relationship Some 1
Family history of Steinert myotonic dystrophy (situation) Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Some 1
Family history of Steinert myotonic dystrophy (situation) Subject relationship context (attribute) persoon in familie van zorgafnemer false Inferred relationship Some 1
Family history of Steinert myotonic dystrophy (situation) Is a FH: Cong. orthopedic anomaly false Inferred relationship Some
Family history of Steinert myotonic dystrophy (situation) Is a Family history of hereditary disease (situation) true Inferred relationship Some
Family history of Steinert myotonic dystrophy (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

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