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77016009: Amyoplasia congenita disruptive sequence (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
127855010 Amyoplasia congenita disruptive sequence en Synonym Active Entire term case insensitive SNOMED CT core module
127856011 Myodystrophia foetalis deformans en Synonym Active Entire term case insensitive SNOMED CT core module
127857019 Classic arthrogryposis en Synonym Active Entire term case insensitive SNOMED CT core module
127859016 Myodystrophia fetalis deformans en Synonym Active Entire term case insensitive SNOMED CT core module
127861013 Congenital arthromyodysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
127862018 Myophagism congenita en Synonym Active Entire term case insensitive SNOMED CT core module
127863011 Amyoplasia congenita en Synonym Active Entire term case insensitive SNOMED CT core module
817800016 Amyoplasia congenita disruptive sequence (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

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 Existential restriction modifier
Amyoplasia congenita disruptive sequence Is a Arthrogryposis true Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Associated morphology Congenital contracture false Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 3
Amyoplasia congenita disruptive sequence Finding site Brain structure false Inferred relationship Existential restriction modifier 3
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Associated morphology Contracture false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Is a Muscle contracture false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 4
Amyoplasia congenita disruptive sequence Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings true Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 4
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 4
Amyoplasia congenita disruptive sequence Associated morphology Contracture true Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Amyoplasia congenita disruptive sequence Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 3
Amyoplasia congenita disruptive sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Associated morphology Contracture false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Finding site Joint structure false Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Is a Congenital anomaly of joint false Inferred relationship Existential restriction modifier
Amyoplasia congenita disruptive sequence Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Amyoplasia congenita disruptive sequence Has interpretation Decreased true Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Interprets Range of joint movement true Inferred relationship Existential restriction modifier 2
Amyoplasia congenita disruptive sequence Finding site Structure of joint region true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Lethal arthrogryposis co-occurrent with anterior horn cell disease Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
X-linked distal arthrogryposis multiplex congenita Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Van den Ende-Gupta syndrome Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Adducted thumbs and arthrogryposis syndrome Christian type Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Arthrogryposis multiplex congenita and whistling face syndrome Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Intellectual disability, developmental delay, contracture syndrome Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Arthrogryposis hyperkeratosis syndrome lethal form Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Autosomal recessive myogenic arthrogryposis multiplex congenita Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Hypomyelination neuropathy arthrogryposis syndrome Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier
Congenital lethal myopathy Compton North type Is a True Amyoplasia congenita disruptive sequence Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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