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Diseases
Genes (611)
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ABHD5
Cerebral Creatine Deficiency
WRN
Werner Syndrome
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PITX3
Anterior Segment Dysgenesis 1
MC2R
Familial Glucocorticoid Deficiency
PIGA
Paroxysmal Nocturnal Hemoglobinuria 1
FOXE3
Anterior Segment Dysgenesis 1
STX3
Microvillus Inclusion Disease
CD59
Paroxysmal Nocturnal Hemoglobinuria 1
SRD5A2
Alopecia, Androgenetic, 1
AR
Placental Site Trophoblastic Tumor
Alopecia, Androgenetic, 1
PIGT
Paroxysmal Nocturnal Hemoglobinuria 1
PXDN
Anterior Segment Dysgenesis 1
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma
TFE3
Epithelioid Hemangioendothelioma
MRAP
Familial Glucocorticoid Deficiency
YAP1
Epithelioid Hemangioendothelioma