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Diseases
Genes (1283)
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NF1
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Watson Syndrome
Legius Syndrome
Moyamoya Disease 2
Noonan Syndrome 6
Multiple Endocrine Neoplasia, Type Iib
Neurofibromatosis
Neurofibromatosis, Type Ii
PTPN11
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Moyamoya Disease 2
Noonan Syndrome 6
Neurofibromatosis
Seckel Syndrome 2
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
RAF1
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Seckel Syndrome 2
LZTR1
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Neurofibromatosis, Type Iii, Mixed Central And Peripheral
Noonan Syndrome 6
Seckel Syndrome 2
Neurofibromatosis, Type Ii
NF2
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Familial Spinal
Neurofibromatosis, Type Iii, Mixed Central And Peripheral
Neurofibromatosis
Neurofibromatosis, Type Ii
KRAS
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Neurofibromatosis
Seckel Syndrome 2
Mccune-Albright Syndrome
SOS1
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Seckel Syndrome 2
PCNT
Cafe-Au-Lait Spots, Multiple
Moyamoya Disease 2
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
Seckel Syndrome 2
BRAF
Cafe-Au-Lait Spots, Multiple
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Legius Syndrome
Noonan Syndrome 6
Neurofibromatosis
BRCA2
Cafe-Au-Lait Spots, Multiple
Fanconi Anemia, Complementation Group P
Neurofibromatosis, Familial Spinal
Fanconi Anemia, Complementation Group D1
Multiple Endocrine Neoplasia, Type Iib
Bloom Syndrome
RIT1
Leopard Syndrome 1
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Seckel Syndrome 2
SPRED1
Neurofibromatosis, Familial Spinal
Watson Syndrome
Legius Syndrome
Noonan Syndrome 6
Neurofibromatosis
MAP2K2
Cafe-Au-Lait Spots, Multiple
Leopard Syndrome 1
Watson Syndrome
Noonan Syndrome 6
Neurofibromatosis, Type Ii
MAP2K1
Cafe-Au-Lait Spots, Multiple
Leopard Syndrome 1
Noonan Syndrome 6
Neurofibromatosis, Type Ii
ATR
Fanconi Anemia, Complementation Group P
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Seckel Syndrome 2
Bloom Syndrome
CBL
Moyamoya Disease 2
Noonan Syndrome 6
Bloom Syndrome
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
NRAS
Neurofibromatosis, Familial Spinal
Leopard Syndrome 1
Noonan Syndrome 6
BUB1B
Cafe-Au-Lait Spots, Multiple
Mosaic Variegated Aneuploidy Syndrome 2
SHOC2
Leopard Syndrome 1
Moyamoya Disease 2
Noonan Syndrome 6
CENPJ
Russell-Silver Syndrome, X-Linked
Noonan Syndrome 6
Seckel Syndrome 2