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Diseases
Genes (1225)
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GJA1
Oculodentodigital Dysplasia
Heart Arrhythmia
Adenoid Cystic Carcinoma
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
Fg Syndrome
KCNJ8
Cantú Syndrome
Heart Arrhythmia
Enamel-Renal Syndrome
ACADVL
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
MMUT
Methylmalonyl-Coa Mutase Deficiency
SLC12A6
Andermann Syndrome
SLC17A5
Salla Disease
ABCC9
Cantú Syndrome
Heart Arrhythmia
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
PQBP1
Renpenning's Syndrome
RECQL4
Baller–gerold Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
COL12A1
Bethlem Myopathy