Incoming and outgoing links Neurofibromatosis (overview)
Back to articleIncoming links
- Aortic isthmus stenosis
- Autosomal dominant inheritance
- Café-au-lait stain
- Constitutional Mismatch Repair Deficiency Syndrom
- Cylindrome
- Dermadrome
- Eye diseases, skin changes
- Familial cancer syndrome
- Ganglioneuroma
- Gingival hyperplasia
- Interstitial lung diseases
- Irishamartom
- Lead pigmentation of the oral mucosa
- Melanotic spots of the mucous membranes
- Merlin
- Molluscum fibrosum
- Nelson syndrome
- Neurocutaneous syndromes
- Neurofibroma
- Neurofibromatosis noonan syndrome
- Neurofibromatosis, segmental
- Nf
- Pheochromocytoma
- Proteus syndrome
- Recklinghausen, m.
- Schwannom
- Tumor syndromes, hereditary
- Von hippel-lindau syndrome
Outgoing links
- Café-au-lait stain
- Cobb syndrome
- Dystrophia pigmentosa
- Irishamartom
- Knudson hypothesis
- Lentiginosis profusa
- Mccune-albright syndrome
- Merlin
- Mutation
- Nerve sheath tumor malignant peripheral
- Neurofibroma
- Neurofibromatosis central
- Neurofibromatosis noonan syndrome
- Neurofibromatosis peripheral
- Neurofibromatosis, segmental
- Nevus spilus
- NF1 Gene
- NF2 gene
- Wild type