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Advanced Download Gene List
  • CAV3
    • Rippling Muscle Disease 1
    • Rippling Muscle Disease 2
  • TH
    • Tyrosine Hydroxylase Deficiency
    • Pheochromocytoma
  • TBC1D24
    • Doors Syndrome
    • Door Syndrome
  • LMX1B
    • Nail-Patella Syndrome
  • RET
    • Pheochromocytoma
  • MAX
    • Pheochromocytoma
  • VHL
    • Pheochromocytoma
  • TMEM127
    • Pheochromocytoma
  • SDHB
    • Pheochromocytoma
  • SDHD
    • Pheochromocytoma
  • ACO2
    • Infantile Cerebellar-Retinal Degeneration
  • SRPX2
    • Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
  • NALCN
    • Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome
  • PYCR2
    • Leukodystrophy, Hypomyelinating, 10
  • ATP6V1B2
    • Autosomal Dominant Deafness-Onychodystrophy Syndrome
  • GDNF
    • Pheochromocytoma
  • KIF1B
    • Pheochromocytoma
  • PLCB1
    • Early Infantile Epileptic Encephalopathy 12
  • TBX22
    • Congenital Radioulnar Synostosis
  • NF1
    • Fibrous Dysplasia Of Bone
    • Pheochromocytoma

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