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Diseases
Genes (966)
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COL2A1
Spondyloepiphyseal Dysplasia Congenita
TTPA
Familial Isolated Vitamin E Deficiency
LIM2
Cataract 19, Multiple Types
SLC4A11
Corneal Dystrophy And Perceptive Deafness
PQBP1
Renpenning's Syndrome
TNF
Callosity
Asthma Attack
Hypoglycemia
Obstructive Lung Disease
Bronchial Hyperresponsiveness
Pulmonary Edema
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
CCL2
Asthma Attack
Bronchial Hyperresponsiveness
Pulmonary Edema
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
LDHA
Glycogen Storage Disease Xi
NOS3
High-Altitude Pulmonary Edema
Pulmonary Edema
Familial Isolated Vitamin E Deficiency
DLX5
Split-Hand/foot Malformation 3
DLX6
Split-Hand/foot Malformation 3
TP63
Split-Hand/foot Malformation 3
NR3C1
Hypoglycemia
High-Altitude Pulmonary Edema
Obstructive Lung Disease
IGF2
Split-Hand/foot Malformation 3
Klippel-Trenaunay-Weber Syndrome
Hypoglycemia
PTEN
Anisometropia
Hypoglycemia
RB1
Pinealoblastoma
Hypoglycemia
Trilateral Retinoblastoma
ADAM33
Asthma Attack
Bronchial Hyperresponsiveness
ABCC8
Hypoglycemia