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Diseases
Genes (2352)
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BRAF
Prader–willi Syndrome
Thyroid Carcinoma, Hurthle Cell
Monosomy
Neuroendocrine Tumor
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SS18
Synovial Sarcoma
MAGEL2
Prader–willi Syndrome
SNRPN
Prader–willi Syndrome
Microdeletion Syndrome
BCL2
Synovial Sarcoma
Thyroid Carcinoma, Hurthle Cell
Neuroendocrine Tumor
ARX
Epileptic Encephalopathy, Early Infantile, 48
Neuroendocrine Tumor
FKRP
Walker–warburg Syndrome
NKX2-1
Thyroid Carcinoma, Hurthle Cell
Neuroendocrine Tumor
NDN
Prader–willi Syndrome
KRAS
Prader–willi Syndrome
Thyroid Carcinoma, Hurthle Cell
Monosomy
Neuroendocrine Tumor
POMGNT1
Walker–warburg Syndrome
RET
Thyroid Carcinoma, Hurthle Cell
Neuroendocrine Tumor
SLC6A17
Mental Retardation, Autosomal Recessive 48
DAG1
Prader–willi Syndrome
Walker–warburg Syndrome
POMT1
Walker–warburg Syndrome
HDAC4
Thyroid Carcinoma, Hurthle Cell
2q37 Monosomy
VIM
Synovial Sarcoma
Thyroid Carcinoma, Hurthle Cell
Monosomy
FKTN
Walker–warburg Syndrome