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Diseases
Genes (412)
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BRAF
Cardiofaciocutaneous Syndrome
Legius Syndrome
Noonan Syndrome With Multiple Lentigines
MAP2K1
Cardiofaciocutaneous Syndrome
Noonan Syndrome With Multiple Lentigines
PTPN11
Cardiofaciocutaneous Syndrome
Noonan Syndrome With Multiple Lentigines
ABHD5
Cerebral Creatine Deficiency
CTSD
Harlequin Ichthyosis
Cln10 Disease
FOXE1
Bamforth-Lazarus Syndrome
HPS1
Hermansky-Pudlak Syndrome With Pulmonary Fibrosis
ABCA12
Harlequin Ichthyosis
KRAS
Hemihypertrophy
Cardiofaciocutaneous Syndrome
COL11A2
Weissenbacher-Zweymüller Syndrome
RAF1
Hepatitis E
Cardiofaciocutaneous Syndrome
Noonan Syndrome With Multiple Lentigines
MAP2K2
Cardiofaciocutaneous Syndrome
SPRED1
Legius Syndrome
GDAP1
Charcot-Marie-Tooth Disease Type 4a
CA5A
Hyperammonemic Encephalopathy Due To Carbonic Anhydrase Va Deficiency
UBE2A
Mental Retardation, X-Linked, Syndromic, Nascimento Type
FXYD2
Hypomagnesemia 2, Renal
RAD50
Nijmegen Breakage Syndrome-Like Disorder
CTCF
Mental Retardation, Autosomal Dominant 21
HRAS
Hemihypertrophy
Cardiofaciocutaneous Syndrome