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Diseases
Genes (634)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Hepatitis E
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Lumbar Disc Disease
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
TP53
Disseminated Superficial Actinic Porokeratosis
Adenoid Cystic Carcinoma
NOTCH1
Adenoid Cystic Carcinoma
PIK3CA
Adenoid Cystic Carcinoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
MYBL1
Adenoid Cystic Carcinoma
FBXW7
Adenoid Cystic Carcinoma
BCOR
Adenoid Cystic Carcinoma
HRAS
Adenoid Cystic Carcinoma