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Diseases
Genes (327)
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SCN1B
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Childhood Absence Epilepsy
Generalized Epilepsy With Febrile Seizures Plus
OPA3
Costeff Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
ABCC9
Cantú Syndrome
ATP1A3
Autosomal Dominant Optic Atrophy Plus Syndrome
SLC29A3
Histiocytosis-Lymphadenopathy Plus Syndrome
PQBP1
Renpenning's Syndrome
CTC1
Coats Plus Syndrome
CACNA1A
Childhood Absence Epilepsy
SLC20A2
Cyclopia
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
HSPA9
Even-Plus Syndrome
B3GLCT
Peters Plus Syndrome
KCNJ8
Cantú Syndrome
VPS33A
Mucopolysaccharidosis-Plus Syndrome
IFIH1
Singleton Merten Syndrome
SCN1A
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Childhood Absence Epilepsy
GABRG2
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Childhood Absence Epilepsy
PAH
Phenylketonuria