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1208346003: Congenital hydrocephalus, low insertion of umbilicus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4963754012 Palmer Pagon syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4963755013 Congenital hydrocephalus, low insertion of umbilicus syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4963757017 Congenital hydrocephalus, low insertion of umbilicus 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
Congenital hydrocephalus, low insertion of umbilicus syndrome Is a Congenital umbilical defect true Inferred relationship Existential restriction modifier
Congenital hydrocephalus, low insertion of umbilicus syndrome Is a Congenital hydrocephalus true Inferred relationship Existential restriction modifier
Congenital hydrocephalus, low insertion of umbilicus syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Congenital hydrocephalus, low insertion of umbilicus syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Congenital hydrocephalus, low insertion of umbilicus syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Finding site Structure of brain cerebrospinal fluid pathway true Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Associated morphology Dilatation true Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital hydrocephalus, low insertion of umbilicus syndrome Finding site Umbilical structure true Inferred relationship Existential restriction modifier 2
Congenital hydrocephalus, low insertion of umbilicus syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital hydrocephalus, low insertion of umbilicus syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital hydrocephalus, low insertion of umbilicus syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Congenital hydrocephalus, low insertion of umbilicus syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process Pathological developmental process 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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