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Diseases
Genes (596)
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BRAF
Vascular Malformation
Macrotia
Webbed Neck
Langerhans Cell Histiocytosis
EFNB1
Craniofrontonasal Dysplasia
IRF6
Hypodontia
Van Der Woude Syndrome
FGFR2
Macrotia
Apert Syndrome
GRHL3
Van Der Woude Syndrome
BCHE
Butyrylcholinesterase Deficiency
IFIH1
Singleton Merten Syndrome
ALPL
Odontohypophosphatasia
AGGF1
Klippel-Trenaunay-Weber Syndrome
Vascular Malformation
LMNB2
Acquired Partial Lipodystrophy
FREM1
Trigonocephaly
MSX1
Hypodontia
RB1
Pinealoblastoma
Webbed Neck
Trilateral Retinoblastoma
IRX5
Hypodontia
Webbed Neck
MFN2
Benign Symmetric Lipomatosis
DDX58
Singleton Merten Syndrome
PAX9
Hypodontia
Regional Odontodysplasia
PTPRF
Amazia
LTBP3
Hypodontia
TWIST1
Apert Syndrome