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1010636000: Waardenburg syndrome type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4213386014 Waardenburg syndrome type 2 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4213387017 Waardenburg syndrome type 2 en Synonym Active Entire term case sensitive SNOMED CT core module
5143462010 Waardenburg syndrome type II en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Waardenburg syndrome type 2 Is a Waardenburg syndrome true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 2 Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 2 Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 2 Finding site Ear structure false Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 2 Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Waardenburg syndrome type 2 Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Waardenburg syndrome type 2 Is a Congenital oculocutaneous hypopigmentation true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 2 Is a Congenital anomaly of hair true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 2 Finding site Hair structure true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 2 Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 2 Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Waardenburg syndrome type 2 Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group
Ocular albinism with congenital sensorineural deafness Is a False Waardenburg syndrome type 2 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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