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Search 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:
Mouse
Zebrafish
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