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Diseases
Genes (468)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
MC2R
Familial Glucocorticoid Deficiency
STX3
Microvillus Inclusion Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
FUT2
Norovirus Infection
CILP
Lumbar Disc Disease
DDX58
Hepatitis E
Singleton Merten Syndrome
COL9A3
Lumbar Disc Disease
SART3
Disseminated Superficial Actinic Porokeratosis
ASPN
Lumbar Disc Disease
STAR
Cholera
Familial Glucocorticoid Deficiency
COL11A1
Lumbar Disc Disease
DRD5
Blepharospasm