All diseases

OMIM ID
200100
OMIM term:
ABETALIPOPROTEINEMIA; ABL
Alternative terms:
ACANTHOCYTOSIS
BASSEN-KORNZWEIG SYNDROME
APOLIPOPROTEIN B DEFICIENCY
MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN DEFICIENCY
MTP DEFICIENCY
(∗) Location:
4q23  
(†) Associated OMIM genes:
MTP  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/f4x2dq2h