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66042003: Congenital hyperplasia of muscle (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
109670013 Congenital hyperplasia of muscle en Synonym Active Entire term case insensitive SNOMED CT core module
109671012 Doppellendigkeit en Synonym Active Entire term case insensitive SNOMED CT core module
109672017 Congenital muscular hypertrophy en Synonym Active Entire term case insensitive SNOMED CT core module
109673010 Myofibrillar hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
109674016 Double muscles in cattle en Synonym Inactive Only initial character case insensitive SNOMED CT core module
805612013 Congenital hyperplasia of muscle (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hyperplasia of muscle Is a Non-human disorder by body site false Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Finding site Skeletal muscle system structure true Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Finding site Non-human body structure false Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Is a Congenital anomaly of musculoskeletal system true Inferred relationship Existential restriction modifier
Congenital hyperplasia of muscle Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Finding site Skeletal muscle system structure false Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital hyperplasia of muscle Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital hyperplasia of muscle Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier 2
Congenital hyperplasia of muscle Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital hyperplasia of muscle Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 3
Congenital hyperplasia of muscle Finding site Skeletal muscle system structure false Inferred relationship Existential restriction modifier 3
Congenital hyperplasia of muscle Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital hyperplasia of muscle Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome Is a True Congenital hyperplasia of muscle Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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