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Diseases
Genes (836)
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BTK
Agammaglobulinemia, X-Linked
MYO5B
Microvillus Inclusion Disease
NOTCH1
Valvular Heart Disease
Adenoid Cystic Carcinoma
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
TP53
Disseminated Superficial Actinic Porokeratosis
Adenoid Cystic Carcinoma
Epithelioid Hemangioendothelioma
Hypopigmentation
PTEN
Adenoid Cystic Carcinoma
Thrombophlebitis
Lumbar Disc Disease
Protein Losing Enteropathy
HTR2B
Valvular Heart Disease
HRAS
Adenoid Cystic Carcinoma
Hypopigmentation
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
PIK3CA
Adenoid Cystic Carcinoma
Agammaglobulinemia, X-Linked
MYBL1
Adenoid Cystic Carcinoma
FBXW7
Adenoid Cystic Carcinoma
BCOR
Adenoid Cystic Carcinoma
MYB
Adenoid Cystic Carcinoma
NFIB
Adenoid Cystic Carcinoma
CREBBP
Adenoid Cystic Carcinoma
KRT5
Adenoid Cystic Carcinoma
Hypopigmentation
TFE3
Adenoid Cystic Carcinoma
Epithelioid Hemangioendothelioma