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Diseases
Genes (932)
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ATRX
Alpha-Thalassemia Mental Retardation Syndrome
Adenoid Cystic Carcinoma
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
Phyllodes Tumor
FOXP3
Ipex Syndrome
Phyllodes Tumor
TTPA
Familial Isolated Vitamin E Deficiency
FLNA
Fg Syndrome
Emery–dreifuss Muscular Dystrophy
Phyllodes Tumor
Intestinal Neuronal Dysplasia
OPA3
Costeff Syndrome
PQBP1
Renpenning's Syndrome
ABCC9
Cantú Syndrome
FECH
Erythropoietic Protoporphyria
PRPS1
Arts Syndrome
TAF1
Dystonia 3, Torsion, X-Linked
UMOD
Medullary Cystic Kidney Disease
SYNE1
Emery–dreifuss Muscular Dystrophy
SLC20A2
Primary Familial Brain Calcification
UBA1
X-Linked Spinal Muscular Atrophy Type 2
GALE
Galactose Epimerase Deficiency
LMNA
Adenoid Cystic Carcinoma
Emery–dreifuss Muscular Dystrophy
PDGFRB
Primary Familial Brain Calcification
KCNJ8
Cantú Syndrome
TP53
Alpha-Thalassemia Mental Retardation Syndrome
Adenoid Cystic Carcinoma
Phyllodes Tumor
Myotonic Dystrophy