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732956000: Brachydactyly and distal symphalangism 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
3498441013 Sillence syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3498442018 Brachydactyly and distal symphalangism syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3498443011 Brachydactyly and distal symphalangism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brachydactyly and distal symphalangism syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Brachyphalangia false Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Symphalangism false Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Finding site Entire middle phalanx true Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Brachydactyly and distal symphalangism syndrome Associated morphology Congenital ankylosis false Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Finding site Interphalangeal joint structure false Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Associated morphology Abnormally short growth false Inferred relationship Existential restriction modifier 3
Brachydactyly and distal symphalangism syndrome Finding site Entire middle phalanx false Inferred relationship Existential restriction modifier 3
Brachydactyly and distal symphalangism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Brachydactyly and distal symphalangism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Brachydactyly and distal symphalangism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Brachydactyly and distal symphalangism syndrome Is a Distal interphalangeal joint symphalangism true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism syndrome Finding site Structure of distal interphalangeal joint true Inferred relationship Existential restriction modifier 1
Brachydactyly and distal symphalangism syndrome Associated morphology Ankylosis true Inferred relationship Existential restriction modifier 1
Brachydactyly and distal symphalangism syndrome Is a Brachymesophalangia true Inferred relationship Existential restriction modifier
Brachydactyly and distal symphalangism 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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