RASopathy
MONDO:0021060Developmental 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.
Also known as: RASopathy, Ras protein signal transduction disease, disorder of Ras protein signal transduction
101 clinical trials for this condition and its sub-types, 9 tagged with RASopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of RASopathy
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Neurofibromatosis type 1 73 trials
3 sub-types
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Noonan syndrome and Noonan-related syndrome 1 trial · 29 incl. sub-types
6 sub-types
- Noonan syndrome 22 trials · 25 incl. sub-types Sub-types →
- Costello syndrome 7 trials
- Cardiofaciocutaneous syndrome 7 trials Sub-types →
- Legius syndrome 5 trials
- Noonan syndrome with multiple lentigines 3 trials Sub-types →
- Noonan syndrome-like disorder with loose anagen hair 0 trials Sub-types →
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Neurofibromatosis-Noonan syndrome 2 trials
1 sub-type
- Watson syndrome 0 trials
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CBL-related disorder 1 trial
Most studied deeper sub-types
Noonan syndrome 3
(2)
Cardiofaciocutaneous syndrome 1
(1)
Noonan syndrome 5
(1)
Cardiofaciocutaneous syndrome 2
(0)
Cardiofaciocutaneous syndrome 3
(0)
Cardiofaciocutaneous syndrome 4
(0)
LEOPARD syndrome 1
(0)
LEOPARD syndrome 2
(0)
LEOPARD syndrome 3
(0)
Noonan syndrome 1
(0)
Noonan syndrome 10
(0)
Noonan syndrome 11
(0)
Noonan syndrome 12
(0)
Noonan syndrome 13
(0)
Noonan syndrome 14
(0)
Noonan syndrome 2
(0)
Noonan syndrome 4
(0)
Noonan syndrome 6
(0)
Noonan syndrome 7
(0)
Noonan syndrome 8
(0)