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Diseases
Genes (470)
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ABHD5
Cerebral Creatine Deficiency
BTK
Agammaglobulinemia, X-Linked
WRN
Werner Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
PITX3
Anterior Segment Dysgenesis 1
IFIH1
Singleton Merten Syndrome
FOXE3
Anterior Segment Dysgenesis 1
SRD5A2
Alopecia, Androgenetic, 1
TFE3
Epithelioid Hemangioendothelioma
Vascular Tumor
AR
Alopecia, Androgenetic, 1
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma
PXDN
Anterior Segment Dysgenesis 1
YAP1
Epithelioid Hemangioendothelioma
PARP1
Alopecia, Androgenetic, 1
Werner Syndrome
ZFP36
Alopecia, Androgenetic, 1
Vascular Tumor
Familial Isolated Vitamin E Deficiency
PRKAR1A
Alopecia, Androgenetic, 1
Werner Syndrome
DDX58
Singleton Merten Syndrome
SART3
Disseminated Superficial Actinic Porokeratosis