FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

723410002: N syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3424476010 N syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3424477018 N 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
N syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
N syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
N syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
N syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
N syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
N syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
N syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
N syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
N syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
N syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
N syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 2
N syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 2
N syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 3
N syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start