FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

74320008: Woolf's syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
123422011 Woolf's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
814806017 Woolf's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2839481017 Woolf syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Woolf's syndrome Is a Albinism true Inferred relationship Existential restriction modifier
Woolf's syndrome Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Woolf's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Woolf's syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Woolf's syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Woolf's syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
Woolf's syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Woolf's syndrome Finding site Eye region structure false Inferred relationship Existential restriction modifier
Woolf's syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier
Woolf's syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 2
Woolf's syndrome Is a Disorder of tyrosine metabolism true Inferred relationship Existential restriction modifier
Woolf's syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
Woolf's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Woolf's syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Woolf's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Woolf's syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 2
Woolf's syndrome Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1
Woolf's syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Woolf's syndrome Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start