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765146000: Oculocutaneous albinism type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3657192012 Oculocutaneous albinism type 1 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3657193019 Oculocutaneous albinism type 1 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculocutaneous albinism type 1 Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism type 1 Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism type 1 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Is a Oculocutaneous albinism true Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 1 Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 1 Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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