All diseases

OMIM ID
605407
OMIM term:
SEGAWA SYNDROME, AUTOSOMAL RECESSIVE
Alternative terms:
PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE
DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE
DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE
TYROSINE HYDROXYLASE DEFICIENCY
(∗) Location:
11p15.5  
(†) Associated OMIM genes:
TH  
(‡) Associated MGI genes:

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