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Diseases
Genes (555)
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SCN1B
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Generalized Epilepsy With Febrile Seizures Plus
OPA3
Costeff Syndrome
Plantar Reflex
COL1A1
Osteogenesis Imperfecta Type Iii
COL1A2
Osteogenesis Imperfecta Type Iii
SCN2A
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Epileptic Encephalopathy, Early Infantile, 40
ABCC9
Cantú Syndrome
ATP1A3
Autosomal Dominant Optic Atrophy Plus Syndrome
SLC29A3
Histiocytosis-Lymphadenopathy Plus Syndrome
CTC1
Coats Plus Syndrome
HSPA9
Even-Plus Syndrome
B3GLCT
Peters Plus Syndrome
KCNJ8
Cantú Syndrome
UGT1A1
Lucey-Driscoll Syndrome
SCN1A
Generalized Epilepsy With Febrile Seizures Plus, Type 8
Epileptic Encephalopathy, Early Infantile, 40
FGA
Hypodysfibrinogenemia
ARX
Epileptic Encephalopathy, Early Infantile, 40
Plantar Reflex
FGB
Hypodysfibrinogenemia
FGG
Hypodysfibrinogenemia
STN1
Coats Plus Syndrome
CDKL5
Epileptic Encephalopathy, Early Infantile, 40