All diseases

OMIM ID
238700
OMIM term:
HYPERLYSINEMIA
Alternative terms:
LYSINE:ALPHA-KETOGLUTARATE REDUCTASE DEFICIENCY
ALPHA-AMINOADIPIC SEMIALDEHYDE SYNTHASE DEFICIENCY
LYSINE INTOLERANCE
L-LYSINE:NAD-OXIDO-REDUCTASE DEFICIENCY
(∗) Location:
7q31.32  
(†) Associated OMIM genes:
AASS  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/4md81ku1