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Diseases
Genes (205)
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MYO5B
Microvillus Inclusion Disease
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
CILP
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
KDM3B
Metal Toxicity
COL9A3
Lumbar Disc Disease
DDX58
Singleton Merten Syndrome
SART3
Disseminated Superficial Actinic Porokeratosis
ASPN
Lumbar Disc Disease
COL11A1
Lumbar Disc Disease
MARK3
Visual Impairment And Progressive Phthisis Bulbi
TXNRD2
Familial Glucocorticoid Deficiency
NNT
Familial Glucocorticoid Deficiency
THBS2
Lumbar Disc Disease