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722057000: albinisme oculo-cutané type 5 (trouble)


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

Descriptions:

Id Description Lang Type Status Case? Module
1014991000172114 AOC5 - albinisme oculo-cutané type 5 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3330413014 Oculocutaneous albinism type 5 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330414015 Oculocutaneous albinism type 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758121000241116 albinisme oculo-cutané type 5 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
913381000172115 albinisme oculo-cutané type 5 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3330415019 A type of oculocutaneous albinism found in one Pakistani family to date, with characteristics of white skin, golden hair, photophobia, nystagmus, foveal hypoplasia and impaired visual acuity. Affects males and females equally. Mapped to a locus on chromosome 4q24 but the gene has not yet been discovered. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculocutaneous albinism type 5 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) est un(e) (attribut) Oculocutaneous albinism true Inferred relationship Some
Oculocutaneous albinism type 5 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) survenue (attribut) congénital false Inferred relationship Some 5
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 5
Oculocutaneous albinism type 5 (disorder) survenue (attribut) congénital false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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