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75491005: Amyotrophia congenita (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
125385010 Amyotrophia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
816106017 Amyotrophia congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4636731000241117 amyotrophie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophia congenita Is a Muscle atrophy true Inferred relationship Some
Amyotrophia congenita Is a Congenital anomaly of skeletal muscle true Inferred relationship Some
Amyotrophia congenita Associated morphology Atrophy false Inferred relationship Some 1
Amyotrophia congenita Associated morphology Congenital hypoplasia false Inferred relationship Some 2
Amyotrophia congenita Associated morphology Congenital atrophy false Inferred relationship Some 1
Amyotrophia congenita Occurrence Congenital false Inferred relationship Some
Amyotrophia congenita Finding site Skeletal muscle structure true Inferred relationship Some 1
Amyotrophia congenita Is a Congenital malformation false Inferred relationship Some
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 2
Amyotrophia congenita Is a Hypoplasia of muscle true Inferred relationship Some
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 2
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 2
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 2
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 2
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 1
Amyotrophia congenita Finding site Skeletal muscle structure true Inferred relationship Some 2
Amyotrophia congenita Occurrence Congenital false Inferred relationship Some 3
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 3
Amyotrophia congenita Occurrence Congenital false Inferred relationship Some 4
Amyotrophia congenita Finding site Skeletal muscle structure false Inferred relationship Some 4
Amyotrophia congenita Associated morphology Atrophy false Inferred relationship Some 3
Amyotrophia congenita Associated morphology Hypoplasia false Inferred relationship Some 4
Amyotrophia congenita Associated morphology Atrophy true Inferred relationship Some 2
Amyotrophia congenita Occurrence Congenital true Inferred relationship Some 2
Amyotrophia congenita Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Amyotrophia congenita Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Amyotrophia congenita Occurrence Congenital true Inferred relationship Some 1
Amyotrophia congenita Associated morphology Hypoplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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