699300009: Oculofaciocardiodental syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Oculofaciocardiodental syndrome
• \Sex-linked hereditary disorder\X-linked hereditary disease\X-linked dominant hereditary disease\Oculofaciocardiodental syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Oculofaciocardiodental syndrome
• \Developmental disorder\Developmental hereditary disorder\Oculofaciocardiodental syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Oculofaciocardiodental syndrome

Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2983577012	Microphthalmia, cataract, radiculomegaly and septal heart defect	en	Synonym	Active	Case insensitive	SNOMED CT core
2983599016	Oculo-facio-cardio-dental syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2983608013	Microphthalmia syndromic 2	en	Synonym	Active	Case insensitive	SNOMED CT core
2983632018	Oculofaciocardiodental syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2983690011	Oculofaciocardiodental syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start