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Diseases
Genes (971)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Adenomyosis
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
PSMB8
Candle Syndrome
PTEN
Thrombophlebitis
Adenomyosis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
MYH11
Berdon Syndrome
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
CREBBP
Agoraphobia
Adenoid Cystic Carcinoma
CTNS
Cystinosis
PIK3CA
Adenomyosis
Adenoid Cystic Carcinoma
NOTCH1
Adenomyosis
Adenoid Cystic Carcinoma
Melorheostosis