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\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Finding of head region\Globe finding\Disorder of eye\Anomaly of eye\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disorder of head\Disorder of eye region\Disorder of eye\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\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\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\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\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 anomaly\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Congenital disease\Congenital anomaly\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 anomaly\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmia with brain and digit anomaly

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3326417011	Microphthalmia with brain and digit anomaly (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3326421016	Microphthalmia with brain and digit anomaly	en	Synonym	Active	Case insensitive	SNOMED CT core
3326422011	Bakrania Ragge syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3326423018	Syndromic microphthalmia type 6	en	Synonym	Active	Case insensitive	SNOMED CT core
3326424012	This syndrome has characteristics of anophthalmia or microphthalmia, retinal dystrophy, and/or myopia, associated in some cases with cerebral anomalies. It has been described in two families. Polydactyly may also be present. Linkage analysis allowed identification of mutations in the BMP4 gene, which has already been shown to play a role in eye development.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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