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403550004: Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1771476019 Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1782575014 Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Is a Aplasia cutis congenita true Inferred relationship Existential restriction modifier
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Occurrence Congenital false Inferred relationship Existential restriction modifier
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated with Epidermolysis bullosa true Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Finding site Skin part true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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