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403805009: Albinism-deafness syndrome of Tietz (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
1771731015 Albinism-deafness syndrome of Tietz (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1782814010 Albinism-deafness syndrome of Tietz 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
Albinism-deafness syndrome of Tietz Is a Albinism true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Occurrence Congenital false Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Finding site Eye region structure false Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Is a Sensorineural hearing loss, bilateral true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Is a Profound sensorineural hearing loss true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Albinism-deafness syndrome of Tietz Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Albinism-deafness syndrome of Tietz Has interpretation Impaired true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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