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40291001: Mietens syndrome (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
63686016 Mietens syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
776907011 Mietens syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mietens syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Mietens syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Mietens syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
Mietens syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier
Mietens syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 1
Mietens syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Mietens syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Mietens syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Mietens syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 1
Mietens syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Mietens syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Mietens syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Mietens syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Mietens syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Mietens syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 2
Mietens syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
Mietens syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Mietens syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Mietens syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Mietens syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Mietens syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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