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Diseases
Genes (846)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
CTSC
Papillon–lefèvre Syndrome
MYH7
Laing Distal Myopathy
SLC26A2
Atelosteogenesis, Type Ii
NOTCH1
Valvular Heart Disease
Paracoccidioidomycosis
Adenoid Cystic Carcinoma
NRAS
Neurocutaneous Melanosis
Hypopigmentation
HTR2B
Valvular Heart Disease
TP53
Papillon–lefèvre Syndrome
Adenoid Cystic Carcinoma
Hypopigmentation
HRAS
Adenoid Cystic Carcinoma
Hypopigmentation
BRAF
Erdheim–chester Disease
PIK3CA
Erdheim–chester Disease
Adenoid Cystic Carcinoma
EPG5
Hypopigmentation
MYBL1
Adenoid Cystic Carcinoma
FBXW7
Adenoid Cystic Carcinoma
BCOR
Adenoid Cystic Carcinoma
MYB
Adenoid Cystic Carcinoma
NFIB
Adenoid Cystic Carcinoma
CREBBP
Adenoid Cystic Carcinoma