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733606001: Summitt syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3499668012 Summitt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3499669016 Summitt syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3499670015 Summitt's acrocephalosyndactyly 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
Summitt syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Summitt syndrome Is a Acrocephalosyndactyly true Inferred relationship Existential restriction modifier
Summitt syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Summitt syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Summitt syndrome Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier
Summitt syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Summitt syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Summitt syndrome Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 3
Summitt syndrome Finding site Joint structure of suture of skull false Inferred relationship Existential restriction modifier 3
Summitt syndrome Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 4
Summitt syndrome Finding site Digit structure false Inferred relationship Existential restriction modifier 4
Summitt syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Summitt syndrome Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier 1
Summitt syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Summitt syndrome Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Summitt syndrome Finding site Digit structure true Inferred relationship Existential restriction modifier 2
Summitt syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Summitt syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Summitt syndrome Associated morphology Congenital abnormal fusion true Inferred relationship Existential restriction modifier 2
Summitt syndrome 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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