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Diseases
Genes (2243)
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TTPA
Familial Isolated Vitamin E Deficiency
BRCA1
Primary Peritoneal Carcinoma
Childhood Leukemia
Adenoid Cystic Carcinoma
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
PTEN
Primary Peritoneal Carcinoma
Thrombophlebitis
Protein Losing Enteropathy
Childhood Leukemia
Adenoid Cystic Carcinoma
TP53
Primary Peritoneal Carcinoma
Childhood Leukemia
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
LIPA
Acid Lipase Disease
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
IL1B
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
Cystinosis
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
NOTCH1
Childhood Leukemia
Adenoid Cystic Carcinoma
PIK3CA
Childhood Leukemia
Adenoid Cystic Carcinoma
CTNS
Cystinosis