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Diseases
Genes (732)
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TTPA
Familial Isolated Vitamin E Deficiency
PTEN
Hibernoma
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
CHD3
Snijders Blok-Campeau Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
JMJD1C
Cayler Cardiofacial Syndrome
Adenoid Cystic Carcinoma
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
GNAS
Fibrous Dysplasia Of Bone
Heterotopic Ossification
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma