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Diseases
Genes (1050)
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PMM2
Pmm2 Deficiency
Hypertelorism
ASL
Argininosuccinic Aciduria
FOXP2
Foxp2-Related Speech And Language Disorder
FOXG1
Foxg1 Syndrome
GNAQ
Sturge–weber Syndrome
ADGRG1
Bilateral Frontoparietal Polymicrogyria
RBM8A
Tar Syndrome
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
RASA1
Sturge–weber Syndrome
MED12
Phyllodes Tumor
Hypertelorism
BRAF
Hypertelorism
Syringocystadenoma Papilliferum
AP3D1
Albinism
FLNA
Phyllodes Tumor
Hypertelorism
SETD2
Phyllodes Tumor
Hypertelorism
FGFR3
Hypertelorism
Syringocystadenoma Papilliferum
Pterygium Of The Conjunctiva And Cornea
TYR
Albinism
EFNB1
Hypertelorism
MITF
Albinism
KMT2D
Phyllodes Tumor
RARA
Phyllodes Tumor