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722057000: Oculocutaneous albinism type 5 (disorder)


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
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
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
913381000172115 albinisme oculo-cutané type 5 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1014991000172114 AOC5 - albinisme oculo-cutané type 5 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculocutaneous albinism type 5 (disorder) Is a Oculocutaneous albinism true Inferred relationship Some
Oculocutaneous albinism type 5 (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Oculocutaneous albinism type 5 (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) Occurrence Congenital false Inferred relationship Some 5
Oculocutaneous albinism type 5 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) Finding site Skin structure false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Some 5
Oculocutaneous albinism type 5 (disorder) Occurrence Congenital false Inferred relationship Some 6
Oculocutaneous albinism type 5 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) Finding site Skin structure false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) Finding site Eye structure false Inferred relationship Some 4
Oculocutaneous albinism type 5 (disorder) Occurrence Congenital true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Finding site Eye structure true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Occurrence Congenital true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) Finding site Eye structure false Inferred relationship Some 1
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) Finding site Skin structure true Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) Finding site Skin structure false Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Associated morphology Hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 5 (disorder) Associated morphology Hypopigmentation false Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Oculocutaneous albinism type 5 (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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