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Diseases
Genes (1486)
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TTPA
Familial Isolated Vitamin E Deficiency
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
SLC12A6
Andermann Syndrome
TNFAIP3
Haploinsufficiency Of A20
TTN
Limb–girdle Muscular Dystrophy
Squamous-Cell Carcinoma Of The Lung
PQBP1
Renpenning's Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NOTCH1
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
Melorheostosis
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
LMNA
Limb–girdle Muscular Dystrophy
Adenoid Cystic Carcinoma
TP53
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
Myotonic Dystrophy
IFIH1
Singleton Merten Syndrome
GNE
Limb–girdle Muscular Dystrophy
Salla Disease
ACTG2
Berdon Syndrome
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
SGCG
Limb–girdle Muscular Dystrophy