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279082008: Acromesomelic dysplasia group (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
416204018 Acromesomelic dysplasia syndrome en Synonym Active Case insensitive SNOMED CT core
416205017 Acromesomelic dysplasia group en Synonym Active Case insensitive SNOMED CT core
416206016 Acromesomelic dwarfism en Synonym Active Case insensitive SNOMED CT core
416207013 Acromesomelic dysplasia en Synonym Active Case insensitive SNOMED CT core
672321019 Acromesomelic dysplasia group (disorder) en Fully specified name Active Case insensitive SNOMED CT core


16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acromesomelic dysplasia syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Acromesomelic dysplasia syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Acromesomelic dysplasia syndrome Is a Disorder of extremity false Inferred relationship Some
Acromesomelic dysplasia syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Acromesomelic dysplasia syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Acromesomelic dysplasia syndrome Finding site Bone structure false Inferred relationship Some 1
Acromesomelic dysplasia syndrome Occurrence Congenital false Inferred relationship Some 2
Acromesomelic dysplasia syndrome Finding site Bone structure false Inferred relationship Some 2
Acromesomelic dysplasia syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 2
Acromesomelic dysplasia syndrome Finding site Bone structure true Inferred relationship Some 1
Acromesomelic dysplasia syndrome Occurrence Congenital false Inferred relationship Some
Acromesomelic dysplasia syndrome Finding site Skeletal system structure false Inferred relationship Some 1
Acromesomelic dysplasia syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Acromesomelic dysplasia syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Some
Acromesomelic dysplasia syndrome Occurrence Congenital true Inferred relationship Some 1
Acromesomelic dysplasia syndrome Is a Congenital skeletal dysplasia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Trichorhinophalangeal syndrome Is a False Acromesomelic dysplasia syndrome Inferred relationship Some
Geleophysic dysplasia Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Hunter-Thompson dysplasia Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Brachydactyly syndrome type B Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Brachydactyly syndrome type C Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Brachydactyly syndrome type E Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Pseudohypoparathyroidism type I A Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Acrodysostosis Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Grebe syndrome Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Acromesomelic dysplasia Maroteaux type Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Acrocapitofemoral dysplasia Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
8q13 microdeletion syndrome Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Acromicric dysplasia Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Saldino-Mainzer dysplasia Is a False Acromesomelic dysplasia syndrome Inferred relationship Some
Cranioectodermal dysplasia Is a True Acromesomelic dysplasia syndrome Inferred relationship Some
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a False Acromesomelic dysplasia syndrome Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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