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Diseases
Genes (1647)
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FMR1
Fragile X Syndrome
Fg Syndrome
Mucopolysaccharidosis Type 2
X-Linked Intellectual Disability
CHM
Choroideremia
X-Linked Intellectual Disability
TP53
Peutz–jeghers Syndrome
Li–fraumeni Syndrome
Machado–joseph Disease
X-Linked Intellectual Disability
DMD
Duchenne And Becker Muscular Dystrophy
Heart Arrhythmia
Mcleod Neuroacanthocytosis Syndrome
Limb–girdle Muscular Dystrophy
X-Linked Intellectual Disability
IDS
Fragile X Syndrome
Heart Arrhythmia
Mucopolysaccharidosis Type 2
STK11
Peutz–jeghers Syndrome
ABCD1
X-Linked Adrenoleukodystrophy
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
XK
Mcleod Neuroacanthocytosis Syndrome
X-Linked Intellectual Disability
KCNJ8
Cantú Syndrome
Heart Arrhythmia
GNAS
Fibrous Dysplasia Of Bone
Peutz–jeghers Syndrome
Progressive Osseous Heteroplasia
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
LMNA
Fragile X Syndrome
Duchenne And Becker Muscular Dystrophy
Heart Arrhythmia
Limb–girdle Muscular Dystrophy
SLC12A6
Andermann Syndrome
MED12
Fragile X Syndrome
Fg Syndrome
X-Linked Intellectual Disability
PTEN
Fragile X Syndrome
Peutz–jeghers Syndrome
Proteus-Like Syndrome
Li–fraumeni Syndrome
PTPN11
Metachondromatosis
Heart Arrhythmia
ABCC9
Cantú Syndrome
Heart Arrhythmia
INPP5E
Joubert Syndrome
SLC17A5
Salla Disease