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723163000: Basal epidermolysis bullosa simplex (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334762019 Basal epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334763012 Basal epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334762019 Basal epidermolysis bullosa simplex (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334762019 Basal epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334763012 Basal epidermolysis bullosa simplex en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334763012 Basal epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
947781000172119 epidermolyse bulleuse simple basale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
947781000172119 epidermolyse bulleuse simple basale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Basal epidermolysis bullosa simplex (disorder) Is a Epidermolysis bullosa simplex true Inferred relationship Existential restriction modifier (core metadata concept)
Basal epidermolysis bullosa simplex (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Basal epidermolysis bullosa simplex (disorder) Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Basal epidermolysis bullosa simplex (disorder) Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Basal epidermolysis bullosa simplex (disorder) Associated morphology Epidermolysis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Basal epidermolysis bullosa simplex (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Basal epidermolysis bullosa simplex (disorder) Finding site Stratum germinativum false Inferred relationship Existential restriction modifier (core metadata concept) 4
Basal epidermolysis bullosa simplex (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Basal epidermolysis bullosa simplex (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Basal epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Basal epidermolysis bullosa simplex (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Basal epidermolysis bullosa simplex (disorder) Finding site Stratum germinativum true Inferred relationship Existential restriction modifier (core metadata concept) 1
Basal epidermolysis bullosa simplex (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Basal epidermolysis bullosa simplex (disorder) Associated morphology Epidermolysis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Epidermolysis bullosa simplex with muscular dystrophy Is a True Basal epidermolysis bullosa simplex (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Keratin 14 related epidermolysis bullosa simplex (disorder) Is a True Basal epidermolysis bullosa simplex (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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