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Diseases
Genes (1404)
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NF1
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis-Noonan Syndrome
Neurofibromatosis, Type I
Legius Syndrome
Cafe-Au-Lait Spots, Multiple
Moyamoya Disease 2
Neurofibromatosis, Type Ii
PTPN11
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
Russell-Silver Syndrome, X-Linked
Moyamoya Disease 2
RAF1
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Russell-Silver Syndrome, X-Linked
LZTR1
Noonan Syndrome 6
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Neurofibromatosis, Type Iii, Mixed Central And Peripheral
Neurofibromatosis, Type Ii
KRAS
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Cafe-Au-Lait Spots, Multiple
Russell-Silver Syndrome, X-Linked
Mccune-Albright Syndrome
BRAF
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Legius Syndrome
Cafe-Au-Lait Spots, Multiple
Xeroderma Pigmentosum, Complementation Group F
SOS1
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Russell-Silver Syndrome, X-Linked
NF2
Neurofibromatosis, Type I
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Type Iii, Mixed Central And Peripheral
Neurofibromatosis, Type Ii
BRCA2
Fanconi Anemia, Complementation Group Q
Neurofibromatosis, Type I
Cafe-Au-Lait Spots, Multiple
Fanconi Anemia, Complementation Group D1
Bloom Syndrome
SPRED1
Noonan Syndrome 6
Neurofibromatosis-Noonan Syndrome
Neurofibromatosis, Type I
Legius Syndrome
RIT1
Noonan Syndrome 6
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
MAP2K2
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis-Noonan Syndrome
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Type Ii
MAP2K1
Noonan Syndrome 6
Leopard Syndrome 1
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Type Ii
CBL
Noonan Syndrome 6
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
Moyamoya Disease 2
Bloom Syndrome
NRAS
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Xeroderma Pigmentosum, Complementation Group F
SHOC2
Noonan Syndrome 6
Leopard Syndrome 1
Moyamoya Disease 2
BUB1B
Mosaic Variegated Aneuploidy Syndrome 2
Cafe-Au-Lait Spots, Multiple
HRAS
Noonan Syndrome 6
Leopard Syndrome 1
Neurofibromatosis, Type I
Xeroderma Pigmentosum, Complementation Group F
Mccune-Albright Syndrome
PCNT
Cafe-Au-Lait Spots, Multiple
Moyamoya Disease 2
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
BLM
Fanconi Anemia, Complementation Group Q
Bloom Syndrome