Preferred Name |
Abetalipoproteinemia |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84525 |
code |
C84525 |
DEFINITION |
An autosomal recessive disorder characterized by defective absorption of dietary fat, cholesterol and fat-soluble vitamins. It results in multiple vitamin deficiencies. Signs and symptoms include failure to thrive, diarrhea, steatorrhea, acanthocytosis and ataxia. |
label |
Abetalipoproteinemia |
Preferred_Name |
Abetalipoproteinemia |
prefixIRI |
C84525 |
prefLabel |
Abetalipoproteinemia |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0000744 |
subClassOf |