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1010712009: Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder)


Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4213648012 Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4213649016 EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
4213650016 Autosomal dominant Emery-Dreifuss muscular dystrophy en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant Emery-Dreifuss muscular dystrophy Is a Emery-Dreifuss muscular dystrophy true Inferred relationship Some
Autosomal dominant Emery-Dreifuss muscular dystrophy Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant Emery-Dreifuss muscular dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant Emery-Dreifuss muscular dystrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant Emery-Dreifuss muscular dystrophy Clinical course Progressive true Inferred relationship Some 2
Autosomal dominant Emery-Dreifuss muscular dystrophy Is a Hereditary progressive muscular dystrophy true Inferred relationship Some
Autosomal dominant Emery-Dreifuss muscular dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Some

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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