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Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disease · Disease by molecular mechanism
RASopathy
Developmental syndromes caused by germline mutations (or in rare cases by somatic mosaicism) in genes that alter the Ras subfamily and mitogen-activated protein kinases that control signal transduction.
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Neurofibromatosis type 1 73 trials Sub-types →
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Noonan syndrome and Noonan-related syndrome 1 trial · 28 incl. sub-types Sub-types →
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CBL-related disorder 1 trial