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Diseases
Genes (1096)
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MYO15A
Deafness, Autosomal Recessive 3
SMN1
Proximal Spinal Muscular Atrophy Type 3
Duchenne Muscular Dystrophy
DMD
Sleep Apnea
Cushing's Disease
Duchenne Muscular Dystrophy
AGL
Pompe Disease
Glycogen Storage Disease Type Iii
GAA
Pompe Disease
TFAP2A
Branchiooculofacial Syndrome
PIK3CD
Activated Pi3k Delta Syndrome
Tonsil Carcinoma
SLC20A2
Primary Familial Brain Calcification
SMN2
Proximal Spinal Muscular Atrophy Type 3
Duchenne Muscular Dystrophy
PDGFRB
Primary Familial Brain Calcification
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
EDN1
Auriculocondylar Syndrome 3
CRH
Cushing's Disease
CCDC50
Deafness, Autosomal Dominant 44
TNF
Allergic Contact Dermatitis
Pompe Disease
Felty's Syndrome
Duchenne Muscular Dystrophy
Latent Tuberculosis
PDGFB
Primary Familial Brain Calcification
IFNG
Allergic Contact Dermatitis
Duchenne Muscular Dystrophy
Latent Tuberculosis
IL6
Aseptic Meningitis
Allergic Contact Dermatitis
Sleep Apnea
Pompe Disease
Cushing's Disease
Duchenne Muscular Dystrophy
SPP1
Allergic Contact Dermatitis
Duchenne Muscular Dystrophy
Latent Tuberculosis