All diseases

OMIM ID
606407
OMIM term:
HYPOTONIA-CYSTINURIA SYNDROME
Alternative terms:
CYSTINURIA WITH MITOCHONDRIAL DISEASE
HOMOZYGOUS 2p16 DELETION SYNDROME, FORMERLY HOMOZYGOUS 2p21 DELETION SYNDROME, INCLUDED
(∗) Location:
2p21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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