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279082008: Acromesomelic dysplasia group (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
416204018 Acromesomelic dysplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
416205017 Acromesomelic dysplasia group en Synonym Active Entire term case insensitive SNOMED CT core module
416206016 Acromesomelic dwarfism en Synonym Active Entire term case insensitive SNOMED CT core module
416207013 Acromesomelic dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
672321019 Acromesomelic dysplasia group (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

16 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acromesomelic dysplasia group Is a Congenital skeletal dysplasia true Inferred relationship Existential restriction modifier
Acromesomelic dysplasia group Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Occurrence Congenital false Inferred relationship Existential restriction modifier
Acromesomelic dysplasia group Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
Acromesomelic dysplasia group Is a Disorder of extremity false Inferred relationship Existential restriction modifier
Acromesomelic dysplasia group Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Acromesomelic dysplasia group Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Acromesomelic dysplasia group Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Acromesomelic dysplasia group Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Acromesomelic dysplasia group Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Acromicric dysplasia Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Saldino-Mainzer dysplasia Is a False Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Cranioectodermal dysplasia Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a False Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Trichorhinophalangeal syndrome Is a False Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Geleophysic dysplasia Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type I A Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Acrodysostosis Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Grebe syndrome Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Acromesomelic dysplasia Hunter-Thompson type Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Brachydactyly syndrome type B Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Brachydactyly syndrome type C Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Brachydactyly syndrome type E Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Acromesomelic dysplasia Maroteaux type Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Acrocapitofemoral dysplasia Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
8q13 microdeletion syndrome Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a True Acromesomelic dysplasia group Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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