FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

237919007: Minimal pigment 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
356582018 Minimal pigment oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356583011 Platinum oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626719010 Minimal pigment oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
356582018 Minimal pigment oculocutaneous albinism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356582018 Minimal pigment oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356583011 Platinum oculocutaneous albinism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356583011 Platinum oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626719010 Minimal pigment oculocutaneous albinism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626719010 Minimal pigment oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
545521000274117 Okulokutaner Platin-Albinismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
551331000274111 Minimal-pigmentierter okulokutaner Albinismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
545521000274117 Okulokutaner Platin-Albinismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
551331000274111 Minimal-pigmentierter okulokutaner Albinismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Minimal pigment oculocutaneous albinism Is a Tyrosinase-negative oculocutaneous albinism true Inferred relationship Existential restriction modifier (core metadata concept)
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Minimal pigment oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Minimal pigment oculocutaneous albinism Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Minimal pigment oculocutaneous albinism Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Minimal pigment oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Minimal pigment oculocutaneous albinism Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Finding site Eye structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal pigment oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start