FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

74320008: Woolf-syndroom (aandoening)


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
123422011 Woolf's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
814806017 Woolf's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2839481017 Woolf syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6071221000146116 syndroom van Woolf nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10673031000146114 Woolf-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10673041000146118 Woolf-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Woolf's syndrome Is a Albinism true Inferred relationship Some
Woolf's syndrome Associated morphology Congenital deficiency false Inferred relationship Some
Woolf's syndrome Occurrence Congenital false Inferred relationship Some
Woolf's syndrome Finding site Structure of skin region false Inferred relationship Some 1
Woolf's syndrome Associated morphology congenitale hypopigmentatie false Inferred relationship Some 2
Woolf's syndrome Finding site Eye structure false Inferred relationship Some
Woolf's syndrome Finding site Skin structure false Inferred relationship Some 3
Woolf's syndrome Finding site Eye region structure (body structure) false Inferred relationship Some
Woolf's syndrome Associated morphology congenitale hypopigmentatie false Inferred relationship Some
Woolf's syndrome Finding site Eye structure false Inferred relationship Some 2
Woolf's syndrome Is a Disorder of tyrosine metabolism true Inferred relationship Some
Woolf's syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Some
Woolf's syndrome Occurrence Congenital true Inferred relationship Some 1
Woolf's syndrome Associated morphology congenitale hypopigmentatie false Inferred relationship Some 1
Woolf's syndrome Occurrence Congenital false Inferred relationship Some 2
Woolf's syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Some 2
Woolf's syndrome Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Woolf's syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Woolf's syndrome Associated morphology Hypopigmentation false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start