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Diseases
Genes (1506)
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FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Fragile X Syndrome
Renpenning's Syndrome
Fragile Xe Syndrome
Fragile X-Associated Primary Ovarian Insufficiency
Fg Syndrome
AFF2
Fragile X Syndrome
Fragile Xe Syndrome
DMD
Duchenne Muscular Dystrophy
X-Linked Recessive Ocular Albinism
BTK
X-Linked Agammaglobulinemia
PHOX2B
Ondine Syndrome
Pinealoblastoma
FAS
Autoimmune Lymphoproliferative Syndrome
PQBP1
Ankylosis
Renpenning's Syndrome
FASLG
Autoimmune Lymphoproliferative Syndrome
GPR143
X-Linked Recessive Ocular Albinism
MED12
Fragile X Syndrome
Fg Syndrome
HBB
Beta-Thalassemia
RET
Duchenne Muscular Dystrophy
Ondine Syndrome
APP
Fragile X Syndrome
Duchenne Muscular Dystrophy
Fragile Xe Syndrome
BDNF
Fragile X Syndrome
Ondine Syndrome
GDNF
Duchenne Muscular Dystrophy
Ondine Syndrome
ASCL1
Ondine Syndrome
EDN3
Ondine Syndrome
SMARCD1
Foot Deformity
Hand Deformity
PIGB
Foot Deformity
Hand Deformity
FGFR2
Fibrolamellar Hepatocellular Carcinoma
Hallux Varus
Ankylosis
Joint Stiffness