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Diseases
Genes (688)
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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
NGLY1
Ngly1 Deficiency
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
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
CTNS
Cystinosis
SYCP3
Spermatogenesis Arrest
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis
PIK3CA
Social (Pragmatic) Communication Disorder
Adenoid Cystic Carcinoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma