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52616002: Freeman-Sheldon syndrome (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
87570012 Freeman-Sheldon syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
87571011 Whistling face syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
790645014 Freeman-Sheldon syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3425566016 Distal arthrogryposis type 2A en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Freeman-Sheldon syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Finding site Face structure false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Congenital anomaly of face bones true Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Finding site Bone structure of face false Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Finding site Bone structure of face false Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Finding site Bone structure of face true Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Is a Distal arthrogryposis syndrome true Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Associated morphology Contracture true Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Finding site Joint structure false Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Freeman-Sheldon syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Is a Congenital anomaly of bone and joint false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Is a Inherited arthrogryposis false Inferred relationship Existential restriction modifier
Freeman-Sheldon syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Freeman-Sheldon syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Interprets Range of joint movement true Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Finding site Structure of joint region true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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