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Diseases
Genes (345)
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MYO5A
Griscelli Syndrome Type 3
Depigmentation
Elejalde Syndrome
TFR2
Haemochromatosis Type 3
TTPA
Familial Isolated Vitamin E Deficiency
RAB27A
Depigmentation
Griscelli Syndrome Type 2
PMM2
Pmm2 Deficiency
MLPH
Griscelli Syndrome Type 3
Depigmentation
IFIH1
Singleton Merten Syndrome
WDR45
Neurodegeneration With Brain Iron Accumulation
MITF
Melanosis
Incontinentia Pigmenti Achromians
Depigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
EPG5
Depigmentation
PANK2
Neurodegeneration With Brain Iron Accumulation
KRT14
Incontinentia Pigmenti Achromians
Depigmentation
DDX58
Singleton Merten Syndrome
SASH1
Generalized Lentiginosis
Depigmentation
TYR
Melanosis
Lentiginosis
Depigmentation
GLI3
Depigmentation
RHOA
Depigmentation
ALDH2
Melanosis
XPC
Melanosis
Poikiloderma
Depigmentation