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Diseases
Genes (1073)
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SALL4
Holt–oram Syndrome
Duane-Radial Ray Syndrome
MED12
Fg Syndrome
Phyllodes Tumor
Alpha-Thalassemia Mental Retardation Syndrome
TBX5
Holt–oram Syndrome
FOXP3
Ipex Syndrome
Phyllodes Tumor
TTPA
Familial Isolated Vitamin E Deficiency
FBN2
Congenital Contractural Arachnodactyly
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
Phyllodes Tumor
Vascular Malformation
FGFR2
Jackson–weiss Syndrome
Congenital Contractural Arachnodactyly
RECQL4
Baller–gerold Syndrome
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
FAM20A
Enamel-Renal Syndrome
FGFR1
Jackson–weiss Syndrome
Congenital Contractural Arachnodactyly
Phyllodes Tumor
UBA1
X-Linked Spinal Muscular Atrophy Type 2
IFIH1
Singleton Merten Syndrome
ALPL
Hypophosphatasia
OFD1
Orofaciodigital Syndrome 1
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TNFSF11
Fibrous Dysplasia Of Bone
Osteopetrosis
Hypophosphatasia