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722058005: Oculocutaneous albinism type 6 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330416018 Oculocutaneous albinism type 6 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3330417010 Oculocutaneous albinism type 6 en Synonym Active Case insensitive SNOMED CT core
3330418017 A type of oculocutaneous albinism recently discovered in one Chinese family, with characteristics of light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity. Caused by mutations in the SLC24A5 gene (15q21.1). en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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