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Diseases
Genes (881)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
MMP21
Situs Ambiguus
ACVR2B
Situs Ambiguus
DMPK
Myotonic Dystrophy
ZIC3
Situs Ambiguus
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
NODAL
Situs Ambiguus
CFAP53
Situs Ambiguus
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma