721878003: Microphthalmia with brain and digit anomaly (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Head finding\...
• \Finding of head region\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Finding of head region\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Eye / vision finding\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system\Microphthalmia with brain and digit anomaly
• \Eye / vision finding\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Microphthalmia with brain and digit anomaly
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Microphthalmia with brain and digit anomaly
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Developmental disorder\Developmental hereditary disorder\Microphthalmia with brain and digit anomaly
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly

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
3326417011	Microphthalmia with brain and digit anomaly (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3326421016	Microphthalmia with brain and digit anomaly	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3326422011	Bakrania Ragge syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3326423018	Syndromic microphthalmia type 6	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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