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Diseases
Genes (566)
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KRAS
Ror2-Related Robinow Syndrome
Noonan Syndrome
Peutz–jeghers Syndrome
PTPN11
X-Linked Lymphoproliferative Disease
Ror2-Related Robinow Syndrome
Noonan Syndrome
RAF1
Ror2-Related Robinow Syndrome
Noonan Syndrome
SOS1
Ror2-Related Robinow Syndrome
Noonan Syndrome
ABHD5
Cerebral Creatine Deficiency
LZTR1
Ror2-Related Robinow Syndrome
Noonan Syndrome
RIT1
Ror2-Related Robinow Syndrome
Noonan Syndrome
NF1
Multiple Endocrine Neoplasia Type 2
Watson Syndrome
Noonan Syndrome
CHM
Choroideremia
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
SH2D1A
X-Linked Lymphoproliferative Disease
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
STK11
Peutz–jeghers Syndrome
LCAT
Fish-Eye Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
MAP2K2
Watson Syndrome
Noonan Syndrome
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
PTEN
Multiple Endocrine Neoplasia Type 2
Proteus-Like Syndrome
Noonan Syndrome
Peutz–jeghers Syndrome
GORAB
Gerodermia Osteodysplastica
Alopecia, Androgenetic, 1
RET
Choroideremia
Multiple Endocrine Neoplasia Type 2