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Diseases
Genes (827)
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TTPA
Familial Isolated Vitamin E Deficiency
MED12
Social (Pragmatic) Communication Disorder
Fg Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
PTEN
Social (Pragmatic) Communication Disorder
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis
PIK3CA
Social (Pragmatic) Communication Disorder
Adenoid Cystic Carcinoma
COL9A2
Stickler Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma