All diseases

OMIM ID
253270
OMIM term:
HOLOCARBOXYLASE SYNTHETASE DEFICIENCY
Alternative terms:
HLCS DEFICIENCY
MULTIPLE CARBOXYLASE DEFICIENCY, NEONATAL FORM
MULTIPLE CARBOXYLASE DEFICIENCY, EARLY ONSET
(∗) Location:
21q22.13  
(†) Associated OMIM genes:
HLCS  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3nxkwsz5