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389167007: Acromesomelic dysplasia Hunter-Thompson type (disorder)


Status: current, Primitive. Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1483219011 Hunter-Thompson dysplasia en Synonym Active Case sensitive SNOMED CT core
4591525019 Acromesomelic dysplasia Hunter-Thompson type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4591527010 Acromesomelic dysplasia Hunter-Thompson type en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hunter-Thompson dysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Hunter-Thompson dysplasia Associated morphology Dysplasia true Inferred relationship Some 1
Hunter-Thompson dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
Hunter-Thompson dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Hunter-Thompson dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Hunter-Thompson dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Hunter-Thompson dysplasia Is a Acromesomelic dysplasia syndrome true Inferred relationship Some
Hunter-Thompson dysplasia Occurrence Congenital false Inferred relationship Some
Hunter-Thompson dysplasia Finding site Bone structure false Inferred relationship Some 1
Hunter-Thompson dysplasia Finding site Musculoskeletal structure of limb false Inferred relationship Some
Hunter-Thompson dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Hunter-Thompson dysplasia Finding site Bone structure true Inferred relationship Some 1
Hunter-Thompson dysplasia Occurrence Congenital false Inferred relationship Some 2
Hunter-Thompson dysplasia Finding site Bone structure false Inferred relationship Some 2
Hunter-Thompson dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 2
Hunter-Thompson dysplasia Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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