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Diseases
Genes (1315)
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PTPN11
Metachondromatosis
Protein Losing Enteropathy
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
PQBP1
X-Linked Intellectual Disability
Renpenning's Syndrome
CHM
Choroideremia
X-Linked Intellectual Disability
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
PTEN
Proteus-Like Syndrome
Thrombophlebitis
Marinesco–sjögren Syndrome
Protein Losing Enteropathy
Squamous-Cell Carcinoma Of The Lung
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
MAP2K1
Cardiofaciocutaneous Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
RYR1
Malignant Hyperthermia
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
MYO5A
Griscelli Syndrome
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome
Squamous-Cell Carcinoma Of The Lung
TTN
Limb–girdle Muscular Dystrophy
Squamous-Cell Carcinoma Of The Lung
TNFAIP3
Haploinsufficiency Of A20
RAB3GAP1
Warburg Micro Syndrome 3
MEGF8
Carpenter Syndrome 1