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Diseases
Genes (1564)
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TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
SLC12A6
Andermann Syndrome
TNFAIP3
Haploinsufficiency Of A20
PQBP1
Renpenning's Syndrome
TTN
Squamous-Cell Carcinoma Of The Lung
Limb–girdle Muscular Dystrophy
SLC17A5
Wilson's Disease
Salla Disease
FAM20A
Enamel-Renal Syndrome
NOTCH1
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
Melorheostosis
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
TP53
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
Myotonic Dystrophy
Wilson's Disease
LMNA
Adenoid Cystic Carcinoma
Limb–girdle Muscular Dystrophy
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
GNE
Limb–girdle Muscular Dystrophy
Salla Disease
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
FGFR2
Squamous-Cell Carcinoma Of The Lung
PIK3CA
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
Salla Disease