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PedAM

Pediatric Disease Annotations & Medicines




Disease tic disorder
Phenotype C0085113|neurofibromatosis
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PubMedID- 23177704 neurofibromatosis is one of several genetic disorders characterized by hyperpigmented skin spots (cafe au lait spots) and multiple neurofibromas.
PubMedID- 22083253 neurofibromatosis is a group of inherited genetic disorders—nf1, nf2, and schwannomatosis—that together affect approximately 100,000 persons in us (http://www.ctf.org/living-with-nf/learn-about-nf.html).

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