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720633009: Syndactyly type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3321602018 Cenani Lenz syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321603011 Cenani Lenz syndactyly en Synonym Active Entire term case sensitive SNOMED CT core module
3321604017 Cenani syndactyly en Synonym Active Entire term case sensitive SNOMED CT core module
3321605016 Syndactyly type 7 en Synonym Active Entire term case insensitive SNOMED CT core module
3321607012 Syndactyly type 7 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Syndactyly type 7 Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Syndactyly type 7 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Syndactyly type 7 Is a Syndactyly true Inferred relationship Existential restriction modifier
Syndactyly type 7 Associated morphology Congenital abnormal fusion true Inferred relationship Existential restriction modifier 1
Syndactyly type 7 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Syndactyly type 7 Finding site Digit structure true Inferred relationship Existential restriction modifier 1
Syndactyly type 7 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Syndactyly type 7 Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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