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Diseases
Genes (378)
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ADAM10
Reticulate Acropigmentation Of Kitamura
Dowling-Degos Disease 1
KRT5
Reticulate Acropigmentation Of Kitamura
Dowling-Degos Disease 1
POFUT1
Reticulate Acropigmentation Of Kitamura
Dowling-Degos Disease 1
POGLUT1
Reticulate Acropigmentation Of Kitamura
Dowling-Degos Disease 1
MYO5B
Microvillus Inclusion Disease
ADAR
Reticulate Acropigmentation Of Kitamura
Dyschromatosis Symmetrica Hereditaria
TTPA
Familial Isolated Vitamin E Deficiency
GNAS
Fibrous Dysplasia Of Bone
Mccune-Albright Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
ATP6
Neuropathy, Ataxia, And Retinitis Pigmentosa
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
PSENEN
Dowling-Degos Disease 1
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
WWTR1
Epithelioid Hemangioendothelioma