Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy   703219008

SNOMED CT code


SNOMED code703219008
nameCerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
statusactive
date introduced2014-07-31
fully specified name(s)Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
synonyms
  • CARASIL syndrome
  • Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
  • Maeda syndrome
  • Nemoto disease
  • Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy
attributes - group1
Finding siteCerebrovascular system structure   28661005
parents
  • Cardiovascular system hereditary disorder   363005004
  • Cerebrovascular disease   62914000
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy   703219008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cerebrovascular disease   62914000
          Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy   703219008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy   703219008

ancestors
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