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77016009: Amyoplasia congenita disruptive sequence (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
127855010 Amyoplasia congenita disruptive sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
127856011 Myodystrophia foetalis deformans en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
127857019 Classic arthrogryposis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
127859016 Myodystrophia fetalis deformans en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
127861013 Congenital arthromyodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
127862018 Myophagism congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
127863011 Amyoplasia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
817800016 Amyoplasia congenita disruptive sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)

10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyoplasia congenita disruptive sequence Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Some
Amyoplasia congenita disruptive sequence Is a Arthrogryposis true Inferred relationship Some
Amyoplasia congenita disruptive sequence Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
Amyoplasia congenita disruptive sequence Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Associated morphology Congenital contracture false Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 3
Amyoplasia congenita disruptive sequence Finding site Brain structure false Inferred relationship Some 3
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Some
Amyoplasia congenita disruptive sequence Is a Disorder of skeletal muscle false Inferred relationship Some
Amyoplasia congenita disruptive sequence Associated morphology Contracture false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Is a Muscle contracture false Inferred relationship Some
Amyoplasia congenita disruptive sequence Associated morphology Congenital malformation false Inferred relationship Some
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 4
Amyoplasia congenita disruptive sequence Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings true Inferred relationship Some
Amyoplasia congenita disruptive sequence Associated morphology Congenital anomaly false Inferred relationship Some 4
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 4
Amyoplasia congenita disruptive sequence Associated morphology Contracture true Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Associated morphology Congenital anomaly false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Some 3
Amyoplasia congenita disruptive sequence Associated morphology Developmental anomaly false Inferred relationship Some 3
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 3
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Associated morphology Contracture false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Is a Congenital anomaly of joint false Inferred relationship Some
Amyoplasia congenita disruptive sequence Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Occurrence Congenital true Inferred relationship Some 1
Amyoplasia congenita disruptive sequence Has interpretation Decreased true Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Interprets Range of joint movement true Inferred relationship Some 2
Amyoplasia congenita disruptive sequence Finding site Structure of joint region true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
X-linked distal arthrogryposis multiplex congenita (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Van den Ende-Gupta syndrome (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Adducted thumbs and arthrogryposis syndrome Christian type (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Arthrogryposis multiplex congenita and whistling face syndrome (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Intellectual disability, developmental delay, contracture syndrome (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Arthrogryposis hyperkeratosis syndrome lethal form (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Hypomyelination neuropathy arthrogryposis syndrome (disorder) Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some
Congenital lethal myopathy Compton North type Is a True Amyoplasia congenita disruptive sequence Inferred relationship Some

This concept is not in any reference sets

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