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240053005: Hereditary myopathy limited to females (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
359649013 Hereditary myopathy limited to females en Synonym Active Entire term case insensitive SNOMED CT core module
629143018 Hereditary myopathy limited to females (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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