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Diseases
Genes (1093)
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CHM
Choroideremia
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
PTEN
Proteus-Like Syndrome
Hypertelorism
Thrombophlebitis
RAB3GAP1
Warburg Micro Syndrome 3
Microphthalmia
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
MYO5A
Griscelli Syndrome
MEGF8
Hypertelorism
Carpenter Syndrome 1
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome
Hypertelorism
PTPN11
Metachondromatosis
Hypertelorism
FOXP2
Foxp2-Related Speech And Language Disorder
NOTCH3
Cadasil
Hypertelorism
FOXG1
Foxg1 Syndrome
RAB18
Warburg Micro Syndrome 3
Microphthalmia
ADGRG1
Bilateral Frontoparietal Polymicrogyria
RAB3GAP2
Warburg Micro Syndrome 3
Microphthalmia
ALS2
Juvenile Primary Lateral Sclerosis
RAB23
Carpenter Syndrome 1
RAC2
Neutrophil Immunodeficiency Syndrome
MGP
Keutel Syndrome