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62144003: Punctate oculocutaneous albinoidism (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
103288015 Punctate oculocutaneous albinoidism en Synonym Active Case insensitive SNOMED CT core
801284017 Punctate oculocutaneous albinoidism (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
Punctate oculocutaneous albinoidism Occurrence Congenital true Inferred relationship Some 1
Punctate oculocutaneous albinoidism Pathological process Pathological developmental process true Inferred relationship Some 1
Punctate oculocutaneous albinoidism Associated morphology Hypopigmentation false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Finding site Eye structure true Inferred relationship Some 2
Punctate oculocutaneous albinoidism Is a Tyrosinase-positive oculocutaneous albinism true Inferred relationship Some
Punctate oculocutaneous albinoidism Pathological process Pathological developmental process true Inferred relationship Some 2
Punctate oculocutaneous albinoidism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Punctate oculocutaneous albinoidism Finding site Eye region structure false Inferred relationship Some
Punctate oculocutaneous albinoidism Is a Oculocutaneous albinoidism false Inferred relationship Some
Punctate oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Finding site Eye structure false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Associated morphology Decreased melanin pigmentation false Inferred relationship Some
Punctate oculocutaneous albinoidism Finding site Eye region structure false Inferred relationship Some
Punctate oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Finding site Skin structure true Inferred relationship Some 1
Punctate oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Occurrence Congenital true Inferred relationship Some 2
Punctate oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Some 3
Punctate oculocutaneous albinoidism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Punctate oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 3
Punctate oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Some 3
Punctate oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Punctate oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Some 3
Punctate oculocutaneous albinoidism Associated morphology Congenital deficiency false Inferred relationship Some
Punctate oculocutaneous albinoidism Finding site Eye structure false Inferred relationship Some
Punctate oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Some
Punctate oculocutaneous albinoidism Finding site Structure of skin region false 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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