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373432000: Bovine hereditary syndactyly (disorder)


    Status: retired, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1198731010 Bovine hereditary syndactyly (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    1211905017 Mule foot deformity en Synonym Active Case insensitive SNOMED CT core
    1490867010 Mule foot en Synonym Active Case insensitive SNOMED CT core
    2672843013 Bovine hereditary syndactyly en Synonym Active Case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Mule foot deformity Is a Congenital anomaly of musculoskeletal system false Inferred relationship Some
    Mule foot deformity Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
    Mule foot deformity Is a Congenital bony fusion of phalanges false Inferred relationship Some
    Mule foot deformity Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Mule foot deformity Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Mule foot deformity Finding site Digit structure false Inferred relationship Some 1
    Mule foot deformity Occurrence Congenital false Inferred relationship Some
    Mule foot deformity Finding site Structure of musculoskeletal system false Inferred relationship Some
    Mule foot deformity Is a Inherited disorder of connective tissue false Inferred relationship Some
    Mule foot deformity Finding site Phalanx structure false Inferred relationship Some 1
    Mule foot deformity Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Mule foot deformity Finding site Phalanx structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    MOVED TO association reference set

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