FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

723163000: Basal epidermolysis bullosa simplex (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3334762019 Basal epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3334763012 Basal epidermolysis bullosa simplex en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

Back to Start