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Diseases
Genes (1358)
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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
SLC17A5
Salla Disease
Wilson's 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
Wilson's Disease
IFIH1
Singleton Merten Syndrome
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
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
PRKDC
Squamous-Cell Carcinoma Of The Lung
Adenoid Cystic Carcinoma
EGFR
Squamous-Cell Carcinoma Of The Lung
Enamel-Renal Syndrome
Adenoid Cystic Carcinoma