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11160000: Brown oculocutaneous albinism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
19329012 Brown oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
19330019 Brown albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
632869015 Brown oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brown oculocutaneous albinism Is a Tyrosinase-positive oculocutaneous albinism true Inferred relationship Some
Brown oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
Brown oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Some
Brown oculocutaneous albinism Finding site Structure of skin region false Inferred relationship Some 2
Brown oculocutaneous albinism Occurrence Congenital false Inferred relationship Some
Brown oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Brown oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 3
Brown oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Brown oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 1
Brown oculocutaneous albinism Due to Disorder of tyrosine metabolism false Inferred relationship Some
Brown oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
Brown oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
Brown oculocutaneous albinism Finding site Skin structure true Inferred relationship Some 1
Brown oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Brown oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Brown oculocutaneous albinism Occurrence Congenital true Inferred relationship Some 2
Brown oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 2
Brown oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 2
Brown oculocutaneous albinism Occurrence Congenital false Inferred relationship Some 3
Brown oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
Brown oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Brown oculocutaneous albinism Occurrence Congenital true Inferred relationship Some 1
Brown oculocutaneous albinism Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Brown oculocutaneous albinism Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Brown oculocutaneous albinism Finding site Eye structure true Inferred relationship Some 2
Brown oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 2
Brown oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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