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Diseases
Genes (242)
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TBC1D24
Doors Syndrome
Door Syndrome
LMX1B
Nail-Patella Syndrome
CAV3
Rippling Muscle Disease 1
ACO2
Infantile Cerebellar-Retinal Degeneration
SRPX2
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
TH
Tyrosine Hydroxylase Deficiency
NALCN
Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome
PYCR2
Leukodystrophy, Hypomyelinating, 10
ATP6V1B2
Autosomal Dominant Deafness-Onychodystrophy Syndrome
PLCB1
Early Infantile Epileptic Encephalopathy 12
TBX22
Congenital Radioulnar Synostosis
SMAD6
Fibrous Dysplasia Of Bone
Congenital Radioulnar Synostosis
ITGB2
Congenital Disorder Of Glycosylation, Type Iic
PTPN22
Giant Cell Arteritis
LDB1
Nail-Patella Syndrome
HMOX1
Carbon Monoxide Poisoning
MBP
Carbon Monoxide Poisoning
NOS1
Carbon Monoxide Poisoning
XDH
Carbon Monoxide Poisoning
COL6A3
Congenital Muscular Dystrophy