FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

720565000: Bohring Opitz syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3321255015 Bohring Opitz syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3321256019 Bohring Opitz syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321257011 C-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321258018 Opitz trigonocephaly-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321259014 Bohring 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
Bohring Opitz syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Bohring Opitz syndrome Is a Developmental delay true Inferred relationship Existential restriction modifier
Bohring Opitz syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Bohring Opitz syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Bohring Opitz syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 2
Bohring Opitz syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Bohring Opitz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Bohring Opitz syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
Bohring Opitz syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Bohring Opitz syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Bohring Opitz syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Bohring Opitz syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Bohring Opitz syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Bohring Opitz syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start