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Diseases
Genes (2235)
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MAPT
Frontotemporal Dementia With Parkinsonism-17
Progressive Supranuclear Palsy
PMM2
Pmm2 Deficiency
Muscular Dystrophy
ASL
Argininosuccinic Aciduria
SPAST
Spastic Paraplegia Type 4
TTPA
Familial Isolated Vitamin E Deficiency
CSF3
Linear Scleroderma
Esophageal Cancer
Localized Scleroderma
Miller-Dieker Lissencephaly Syndrome
Hypertrophy
TNF
Fistula
Linear Scleroderma
Osteoglophonic Dysplasia
Esophageal Cancer
Localized Scleroderma
Ureteral Obstruction
Frontotemporal Dementia With Parkinsonism-17
Diverticulum
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
GRN
Esophageal Cancer
Localized Scleroderma
Frontotemporal Dementia With Parkinsonism-17
LMNA
Muscular Dystrophy
Linear Scleroderma
Localized Scleroderma
Frontotemporal Dementia With Parkinsonism-17
FTL
Hyperferritinemia-Cataract Syndrome
PSEN1
Frontotemporal Dementia With Parkinsonism-17
SACS
Autosomal Recessive Spastic Ataxia Of Charlevoix-Saguenay
PQBP1
Renpenning's Syndrome
FGFR1
Osteoglophonic Dysplasia
Esophageal Cancer
DSPP
Dentinogenesis Imperfecta Type 3
RELN
Esophageal Cancer
Lissencephaly With Cerebellar Hypoplasia
CHMP2B
Ureteral Obstruction
Frontotemporal Dementia With Parkinsonism-17
TARDBP
Frontotemporal Dementia With Parkinsonism-17
IFIH1
Singleton Merten Syndrome
AGT
Ureteral Obstruction
Hypertrophy