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Diseases
Genes (783)
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OPN1LW
Blue Cone Monochromatism
PAX3
Congenital Hearing Loss
Waardenburg Syndrome Type I
HOXA13
Hand-Foot-Genital Syndrome
CLN3
Batten Disease
AFG3L2
Spinocerebellar Ataxia Type 28
CP
Aceruloplasminemia
PMM2
Pmm2 Deficiency
TPP1
Batten Disease
Alzheimer Disease 11
GRID2
Spinocerebellar Ataxia, Autosomal Recessive 18
DCTN1
Perry Syndrome
OPN1MW
Blue Cone Monochromatism
ALB
Hyperthyroxinemia, Familial Dysalbuminemic
WDR11
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia
PTEN
Proteus Syndrome
AKT1
Proteus Syndrome
Alzheimer Disease 11
SLC25A19
Amish Lethal Microcephaly
PROKR2
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia
ANOS1
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia
SEC61A1
Hyperuricemic Nephropathy, Familial Juvenile, 4
PMP22
Charcot-Marie-Tooth Disease