FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

4602007: Robin sequence (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
7920012 Robin sequence en Synonym Active Entire term case sensitive SNOMED CT core module
7921011 Micrognathia-glossoptosis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
7922016 Pierre Robin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
783324010 Robin sequence (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1230294017 Pierre Robin association en Synonym Active Entire term case sensitive SNOMED CT core module

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Robin sequence Is a Multisystem disorder O-P false Inferred relationship Existential restriction modifier
Robin sequence Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Robin sequence Occurrence Congenital false Inferred relationship Existential restriction modifier
Robin sequence Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Robin sequence Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Robin sequence Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Robin sequence Finding site Face structure true Inferred relationship Existential restriction modifier 1
Robin sequence Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Robin sequence Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier
Pierre Robin sequence faciodigital anomaly syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier
Intellectual disability, brachydactyly, Pierre Robin syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier
Robin sequence and oligodactyly syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier
Joint contractures, developmental delay, Pierre Robin syndrome Is a True Robin sequence Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start