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Diseases
Genes (899)
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GJA1
Oculodentodigital Dysplasia
Heart Arrhythmia
SALL4
Duane-Radial Ray Syndrome
Heart Arrhythmia
TTPA
Familial Isolated Vitamin E Deficiency
Heart Arrhythmia
COL6A1
Bethlem Myopathy
FMR1
Disinhibition
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
MMUT
Methylmalonyl-Coa Mutase Deficiency
SLC17A5
Salla Disease
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
PQBP1
Renpenning's Syndrome
RECQL4
Baller–gerold Syndrome
IFIH1
Singleton Merten Syndrome
COL12A1
Bethlem Myopathy
CD55
Protein Losing Enteropathy
OPRK1
Heart Arrhythmia
KCNH2
Heart Arrhythmia
MEN1
Glucagonoma
IL6
Fibrous Dysplasia Of Bone
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Heart Arrhythmia
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ACE
Aseptic Meningitis
Heart Arrhythmia