SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital hamartoma  399960008

Ruvalcaba-Myhre syndrome   46011003

SNOMED CT code


SNOMED code46011003
nameRuvalcaba-Myhre syndrome
statusremoved
date introduced2002-01-31
fully specified name(s)Ruvalcaba-Myhre syndrome (disorder)
synonyms
  • Ruvalcaba Myhre Smith syndrome
  • Haemangiomata with macrocephaly and pseudopapilloedema
  • Hemangiomata with macrocephaly and pseudopapilledema
  • Ruvalcaba-Myhre syndrome
parentsCongenital hamartoma   399960008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hamartoma   399960008
          Ruvalcaba-Myhre syndrome   46011003  removed: 2020-07-31

ancestors
sorted most to least specific
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