X-linked hereditary disease
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Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder)
MECP2 related disorder
MECP2 (methyl-cytosine phosphate guanine binding protein-2) disorder
Methyl-CpG (cytosine phosphate guanine) binding protein-2 disorder
Methyl-cytosine phosphate guanine binding protein-2 related disorder
Methyl-CpG binding protein 2 related disorder
Id1296869000
StatusPrimitive
SNOMED CT to ICD-10 extended map
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified
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MECP2 duplication syndrome
PPM-X syndrome
Rett syndrome
Severe neonatal onset encephalopathy with microcephaly