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33979003: Nievergelt's 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
56730016 Nievergelt's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
56731017 Nievergelt-Erb syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
485700013 Mesomelic dysplasia - Nievergelt type en Synonym Active Only initial character case insensitive SNOMED CT core module
765446011 Nievergelt's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2840192018 Nievergelt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nievergelt's syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Nievergelt's syndrome Is a Mesomelic dysplasia true Inferred relationship Existential restriction modifier
Nievergelt's syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Nievergelt's syndrome Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Nievergelt's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Nievergelt's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Nievergelt's syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Nievergelt's syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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