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237918004: Waardenburg syndrome type 3 (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
356581013 Klein-Waardenberg's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2840009017 Klein-Waardenberg syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5143350012 Waardenburg syndrome type 3 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
5143351011 Waardenburg syndrome type 3 en Synonym Active Entire term case sensitive SNOMED CT core module
5143352016 Waardenburg syndrome type III en Synonym Active Entire term case sensitive SNOMED CT core module
5143353014 Waardenburg syndrome with limb anomalies 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
Waardenburg syndrome type 3 Is a Multisystem disorder W-X false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Albinism false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Occurrence Congenital false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Waardenburg syndrome type 3 Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Finding site Eye region structure false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Congenital deficiency of pigment of skin false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Congenital malformation syndromes involving limbs false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Waardenburg syndrome true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Waardenburg syndrome type 3 Has interpretation Decreased true Inferred relationship Existential restriction modifier 4
Waardenburg syndrome type 3 Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Finding site Limb structure true Inferred relationship Existential restriction modifier 1
Waardenburg syndrome type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Waardenburg syndrome type 3 Is a Dystopia canthorum true Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Waardenburg syndrome type 3 Finding site Medial canthus structure true Inferred relationship Existential restriction modifier 5
Waardenburg syndrome type 3 Associated morphology Lateral displacement true Inferred relationship Existential restriction modifier 5
Waardenburg syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Waardenburg syndrome type 3 Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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