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722059002: albinisme oculo-cutané type 7 (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
3330419013 Oculocutaneous albinism type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330420019 Oculocutaneous albinism type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758141000241112 albinisme oculo-cutané type 7 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
907721000172111 AOC7 - albinisme oculo-cutané type 7 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
983731000172115 albinisme oculo-cutané type 7 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3330421015 A form of oculocutaneous albinism with characteristics of skin and hair hypopigmentation, nystagmus and iris transillumination. The prevalence is unknown. It has been discovered in several Faroese families and one patient of Lithuanian origin. Patients have a light skin pigmentation that is reported as lighter than their relatives. Caused by mutation in the C10orf11 gene (10q22.3) encoding a 198 amino acid protein. Currently, little is known about the biological function of this gene in humans and its role in this disease pathogenesis. 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 7 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) est un(e) (attribut) Oculocutaneous albinism true Inferred relationship Some
Oculocutaneous albinism type 7 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 7 (disorder) survenue (attribut) congénital false Inferred relationship Some 5
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 6
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 6
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 5
Oculocutaneous albinism type 7 (disorder) survenue (attribut) congénital false Inferred relationship Some 6
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 4
Oculocutaneous albinism type 7 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) true Inferred relationship Some 2
Oculocutaneous albinism type 7 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 1
Oculocutaneous albinism type 7 (disorder) survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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