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403805009: Albinism-deafness syndrome of Tietz (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
1771731015 Albinism-deafness syndrome of Tietz (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782814010 Albinism-deafness syndrome of Tietz 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
Albinism-deafness syndrome of Tietz (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) perte auditive neurosensorielle, bilatérale true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) Profound sensorineural hearing loss true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) Auditory system hereditary disorder true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) localisation d'une constatation (attribut) structure du système auditif true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) interprète (attribut) Hearing, function (observable entity) true Inferred relationship Some 3
Albinism-deafness syndrome of Tietz (disorder) a pour interprétation (attribut) altéré true Inferred relationship Some 3
Albinism-deafness syndrome of Tietz (disorder) est un(e) (attribut) Albinism true Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Congenital deficiency false Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) survenue (attribut) congénital false Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) localisation d'une constatation (attribut) Eye region structure (body structure) false Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some
Albinism-deafness syndrome of Tietz (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 2
Albinism-deafness syndrome of Tietz (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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