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398071000: Epidermolysis bullosa simplex, Ogna type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1765990017 Epidermolysis bullosa simplex, Ogna type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1777638014 Epidermolysis bullosa simplex, Ogna type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786086018 Epidermolysis bullosa simplex of Ogna en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epidermolysis bullosa simplex, Ogna type (disorder) Is a Autosomal dominant epidermolysis bullosa simplex (disorder) true Inferred relationship Some
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Connective tissue structure false Inferred relationship Some
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Epidermolysis false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Keratolysis false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Blister false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Occurrence Congenital false Inferred relationship Some
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure true Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 2
Epidermolysis bullosa simplex, Ogna type (disorder) Occurrence Congenital false Inferred relationship Some 3
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Epidermolysis bullosa simplex, Ogna type (disorder) Finding site Skin structure false Inferred relationship Some 3
Epidermolysis bullosa simplex, Ogna type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Occurrence Congenital true Inferred relationship Some 1
Epidermolysis bullosa simplex, Ogna type (disorder) Associated morphology Epidermolysis 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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