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403805009: Albinism-deafness syndrome of Tietz (disorder)

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771731015 Albinism-deafness syndrome of Tietz (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
1782814010 Albinism-deafness syndrome of Tietz en Synonym Active Initial character case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Albinism-deafness syndrome of Tietz Pathological process Pathological developmental process true Inferred relationship Some 1
Albinism-deafness syndrome of Tietz Associated morphology Hypopigmentation false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Albinism-deafness syndrome of Tietz Is a Sensorineural hearing loss, bilateral true Inferred relationship Some
Albinism-deafness syndrome of Tietz Is a Congenital sensorineural hearing loss true Inferred relationship Some
Albinism-deafness syndrome of Tietz Is a Profound sensorineural hearing loss true Inferred relationship Some
Albinism-deafness syndrome of Tietz Is a Auditory system hereditary disorder true Inferred relationship Some
Albinism-deafness syndrome of Tietz Finding site Structure of auditory system true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Pathological process Pathological developmental process true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Interprets Hearing true Inferred relationship Some 3
Albinism-deafness syndrome of Tietz Has interpretation Impaired true Inferred relationship Some 3
Albinism-deafness syndrome of Tietz Is a Albinism true Inferred relationship Some
Albinism-deafness syndrome of Tietz Finding site Structure of skin region false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Some
Albinism-deafness syndrome of Tietz Associated morphology Congenital deficiency false Inferred relationship Some
Albinism-deafness syndrome of Tietz Occurrence Congenital false Inferred relationship Some
Albinism-deafness syndrome of Tietz Finding site Eye region structure false Inferred relationship Some
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Finding site Eye structure false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation false Inferred relationship Some
Albinism-deafness syndrome of Tietz Occurrence Congenital true Inferred relationship Some 1
Albinism-deafness syndrome of Tietz Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz Occurrence Congenital true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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