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111388003: Cutis laxa, autosomal dominant (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
178628015 Cutis laxa, autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
630983013 Cutis laxa, autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cutis laxa, autosomal dominant morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
Cutis laxa, autosomal dominant Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Cutis laxa, autosomal dominant survenue (attribut) congénital true Inferred relationship Some 1
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) Connective tissue structure true Inferred relationship Some 1
Cutis laxa, autosomal dominant morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Cutis laxa, autosomal dominant est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
Cutis laxa, autosomal dominant est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Cutis laxa, autosomal dominant morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Cutis laxa, autosomal dominant survenue (attribut) congénital false Inferred relationship Some 2
Cutis laxa, autosomal dominant morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 2
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) appareil locomoteur false Inferred relationship Some
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Cutis laxa, autosomal dominant survenue (attribut) congénital false Inferred relationship Some
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Cutis laxa, autosomal dominant localisation d'une constatation (attribut) Connective tissue false Inferred relationship Some
Cutis laxa, autosomal dominant est un(e) (attribut) Inherited cutis laxa true Inferred relationship Some
Cutis laxa, autosomal dominant est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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