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Diseases
Genes (2422)
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SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
BRAF
Thyroid Carcinoma, Hurthle Cell
Prader–willi Syndrome
Skin Condition
Cognitive Deficit
MAGEL2
Prader–willi Syndrome
SS18
Synovial Sarcoma
SNRPN
Prader–willi Syndrome
NKX2-1
Thyroid Carcinoma, Hurthle Cell
PPARG
Thyroid Carcinoma, Hurthle Cell
Bright's Disease
KRT17
Pachyonychia Congenita
BCL2
Synovial Sarcoma
Thyroid Carcinoma, Hurthle Cell
CCDC6
Thyroid Carcinoma, Hurthle Cell
RET
Thyroid Carcinoma, Hurthle Cell
KRAS
Thyroid Carcinoma, Hurthle Cell
Prader–willi Syndrome
TNF
Synovial Sarcoma
African Trypanosomiasis
Severe Acute Respiratory Syndrome
Thyroid Carcinoma, Hurthle Cell
Prader–willi Syndrome
Bloodstream Infections
Bright's Disease
Salmonellosis
Cognitive Deficit
KRT16
Pachyonychia Congenita
Skin Condition
NDN
Prader–willi Syndrome
AGT
Severe Acute Respiratory Syndrome
Bright's Disease
Cognitive Deficit
Secondary Hypertension
VIM
Synovial Sarcoma
Thyroid Carcinoma, Hurthle Cell
Bloodstream Infections
Salmonellosis
FOXE1
Thyroid Carcinoma, Hurthle Cell
IL6
Synovial Sarcoma
African Trypanosomiasis
Severe Acute Respiratory Syndrome
Thyroid Carcinoma, Hurthle Cell
Prader–willi Syndrome
Bloodstream Infections
Bright's Disease
Cognitive Deficit