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723163000: Basal epidermolysis bullosa simplex (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3334763012 Basal epidermolysis bullosa simplex en Synonym Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Basal epidermolysis bullosa simplex Pathological process Pathological developmental process true Inferred relationship Some 1
Basal epidermolysis bullosa simplex Finding site Stratum germinativum structure true Inferred relationship Some 1
Basal epidermolysis bullosa simplex Occurrence Congenital true Inferred relationship Some 1
Basal epidermolysis bullosa simplex Associated morphology Epidermolysis true Inferred relationship Some 1
Basal epidermolysis bullosa simplex Is a Epidermolysis bullosa simplex true Inferred relationship Some
Basal epidermolysis bullosa simplex Is a Inherited disorder of connective tissue false Inferred relationship Some
Basal epidermolysis bullosa simplex Is a Hereditary disorder of the integument false Inferred relationship Some
Basal epidermolysis bullosa simplex Finding site Connective tissue structure false Inferred relationship Some
Basal epidermolysis bullosa simplex Associated morphology Epidermolysis false Inferred relationship Some 4
Basal epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Some 4
Basal epidermolysis bullosa simplex Finding site Stratum germinativum structure false Inferred relationship Some 4
Basal epidermolysis bullosa simplex Associated morphology Developmental abnormality false Inferred relationship Some 5
Basal epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Some 5
Basal epidermolysis bullosa simplex Finding site Skin structure false Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group
Epidermolysis bullosa simplex with muscular dystrophy Is a True Basal epidermolysis bullosa simplex Inferred relationship Some
KRT14 related epidermolysis bullosa simplex Is a True Basal epidermolysis bullosa simplex Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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