702816000: Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Head finding\...
• \Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Chromosome Xq28 trisomy\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Chromosome Xq28 trisomy\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3006199010	Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3006205015	MECP2 duplication syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3006209014	Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3006219015	Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3009035015	Lubs X-linked mental retardation syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3643143014	Lubs X-linked intellectual disability syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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