Symptoms of Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

Symptoms

The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database.

Signs and Symptoms

Last updated: 1/1/2017

Source: GARD (NIH)1

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Back to: « Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

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Clinical features

Imported from Human Phenotype Ontology (HPO)

Source: GTR (NCBI/NIH)2

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References

  1. Source: GARD (NIH): rarediseases.info.nih.gov/ diseases/ 10424/ cerebral-autosomal-recessive-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy
  2. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C1838577/ 

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