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237919007: Minimal pigment oculocutaneous albinism (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356582018 Minimal pigment oculocutaneous albinism en Synonym Active Case insensitive SNOMED CT core
356583011 Platinum oculocutaneous albinism en Synonym Active Case insensitive SNOMED CT core
626719010 Minimal pigment oculocutaneous albinism (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Minimal pigment oculocutaneous albinism Pathological process Pathological developmental process true Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Pathological process Pathological developmental process true Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Finding site Eye structure true Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Finding site Skin structure true Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 3
Minimal pigment oculocutaneous albinism Occurrence Congenital true Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Occurrence Congenital false Inferred relationship Some 3
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Minimal pigment oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Some
Minimal pigment oculocutaneous albinism Finding site Structure of skin region false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Occurrence Congenital false Inferred relationship Some
Minimal pigment oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
Minimal pigment oculocutaneous albinism Is a Tyrosinase-negative oculocutaneous albinism true Inferred relationship Some
Minimal pigment oculocutaneous albinism 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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