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699300009: Oculofaciocardiodental syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983577012 Microphthalmia, cataract, radiculomegaly and septal heart defect en Synonym Active Entire term case insensitive SNOMED CT core module
2983599016 Oculo-facio-cardio-dental syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2983608013 Microphthalmia syndromic 2 en Synonym Active Entire term case insensitive SNOMED CT core module
2983632018 Oculofaciocardiodental syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2983690011 Oculofaciocardiodental syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2337771000000116 OFCD (oculofaciocardiodental) syndrome en Synonym Active Entire term case sensitive SNOMED CT United Kingdom Edition module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculofaciocardiodental syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Oculofaciocardiodental syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Oculofaciocardiodental syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Oculofaciocardiodental syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Oculofaciocardiodental syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculofaciocardiodental syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Oculofaciocardiodental syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Oculofaciocardiodental syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculofaciocardiodental syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Oculofaciocardiodental syndrome Is a X-linked dominant hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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