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Neurofibromatosis type 1

A clinically heterogeneous, neurocutaneous genetic disorder characterized by cafe-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas.

73 trials tagged with this condition →

Chromosome 17q11.2 deletion syndrome, 1.4Mb 0 trials
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion 0 trials
Neurofibromatosis, familial spinal 0 trials