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1177166006: Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4643796019 Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4643797011 Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Is a Frontonasal dysplasia sequence true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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