Neurocutaneous syndrome
MONDO:0042983A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs.
Also known as: neurocutaneous syndrome, Phacomatoses, Phacomatosis, Phakomatoses, neurocutaneous disorder, neurocutaneous disorders, neuroectodermal dysplasia, neuroectodermal dysplasia syndrome
171 clinical trials for this condition and its sub-types, 2 tagged with Neurocutaneous syndrome itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Neurocutaneous syndrome
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Neurofibromatosis 19 trials · 94 incl. sub-types
5 sub-types
- Neurofibromatosis type 1 73 trials Sub-types →
- NF2-related schwannomatosis 21 trials
- Schwannomatosis 3 trials Sub-types →
- Neurofibromatosis-Noonan syndrome 2 trials Sub-types →
- Neurofibromatosis, type IV, of Riccardi 0 trials
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Tuberous sclerosis 41 trials · 44 incl. sub-types
2 sub-types
- Tuberous sclerosis 1 33 trials
- Tuberous sclerosis 2 2 trials
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Von Hippel-Lindau disease 27 trials
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Sturge-Weber syndrome 8 trials
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Nevoid basal cell carcinoma syndrome 5 trials
2 sub-types
- Basal cell nevus syndrome 1 0 trials
- Basal cell nevus syndrome 2 0 trials
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Neurocutaneous melanocytosis 1 trial
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Wyburn-Mason syndrome 0 trials
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Phakomatosis pigmentokeratotica 0 trials
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Phakomatosis pigmentovascularis 0 trials
3 sub-types
- Phakomatosis cesioflammea 0 trials
- Phakomatosis cesiomarmorata 0 trials
- Phakomatosis spilorosea 0 trials
Most studied deeper sub-types
22q-related schwannomatosis
(0)
Chromosome 17q11.2 deletion syndrome, 1.4Mb
(0)
LZTR1-related schwannomatosis
(0)
Neurofibromatosis, familial spinal
(0)
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
(0)
Neurofibromatosis, type III, mixed central and peripheral
(0)
SMARCB1-related schwannomatosis
(0)
Watson syndrome
(0)