FHIR © HL7.org | Server Home | FHIR Server FHIR Server 4.0.1 | FHIR Version n/a User: [n/a]

74320008: Woolf's syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Woolf's syndrome

\Developmental hereditary disorder\Albinism\Woolf's syndrome

\Disorder of pigmentation (disorder)\Albinism\Woolf's syndrome

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Woolf's syndrome
\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Woolf's syndrome

\Congenital disease (disorder)\Congenital malformation\Albinism\Woolf's syndrome
\Congenital disease (disorder)\Inborn error of metabolism\Albinism\Woolf's syndrome

\Developmental disorder\Developmental hereditary disorder\Albinism\Woolf's syndrome
\Developmental disorder\Congenital malformation\Albinism\Woolf's syndrome

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

Descriptions:

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	Congenital hypopigmentation	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	Congenital hypopigmentation	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	Congenital hypopigmentation	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

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
4395341000172111	Woolf-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4395351000172113	syndroom van Woolf	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)