SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Sex-linked hereditary disorder  82852009

X-linked hereditary disease  128430005

MECP2 related disorder   1296869000

SNOMED CT code


SNOMED code1296869000
nameMECP2 related disorder
statusactive
date introduced2023-12-01
fully specified name(s)Methyl-cytosine phosphate guanine binding protein-2 related disorder (disorder)
synonyms
  • Methyl-CpG (cytosine phosphate guanine) binding protein-2 disorder
  • MECP2 (methyl-cytosine phosphate guanine binding protein-2) disorder
  • Methyl-cytosine phosphate guanine binding protein-2 related disorder
  • Methyl-CpG binding protein 2 related disorder
  • MECP2 related disorder
parentsX-linked hereditary disease   128430005
children
  • Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome   702816000
  • PPM-X syndrome   702356009
  • Rett syndrome   68618008
  • Severe neonatal onset encephalopathy with microcephaly   771303004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              MECP2 related disorder   1296869000

ancestors
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cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

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