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240053005: Hereditary myopathy limited to females (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
359649013 Hereditary myopathy limited to females en Synonym Active Case insensitive SNOMED CT core
629143018 Hereditary myopathy limited to females (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary myopathy limited to females Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Hereditary myopathy limited to females Pathological process Pathological developmental process false Inferred relationship Some 2
Hereditary myopathy limited to females Pathological process Pathological developmental process true Inferred relationship Some 1
Hereditary myopathy limited to females Occurrence Congenital true Inferred relationship Some 1
Hereditary myopathy limited to females Clinical course Progressive true Inferred relationship Some 2
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some
Hereditary myopathy limited to females Associated morphology Congenital anomaly false Inferred relationship Some 2
Hereditary myopathy limited to females Associated morphology Dystrophy true Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure true Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some 3
Hereditary myopathy limited to females Associated morphology Developmental abnormality false Inferred relationship Some 3
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 3
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Is a X-linked limb girdle muscular dystrophy with normal dystrophin true Inferred relationship Some
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some 2

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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