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Neurofibromatosis, type IV, of Riccardi(NF4)

MedGen UID:: 67393
•Concept ID:: C0220695
•: Disease or Syndrome

Synonyms:	Atypical neurofibromatosis; Neurofibromatosis type 4; Neurofibromatosis type 4 of Riccardi; NEUROFIBROMATOSIS, VARIANT FORM(S) OF; NF IV

HPO:	HP:0007524
Monarch Initiative:	MONDO:0008081
OMIM®:	162270

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVNeurofibromatosis, type IV, of Riccardi

Pathological Conditions, Signs and Symptoms
- Pathological process
  - Disease
    - Hereditary disease
      - Hereditary cancer-predisposing syndrome
        Neurofibromatosis
        Neurofibromatosis, type IV, of Riccardi

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Clinical prediction guides

Type 1 neurofibromatosis: selective expression of extracellular matrix genes by Schwann cells, perineurial cells, and fibroblasts in mixed cultures.

Jaakkola S, Peltonen J, Riccardi V, Chu ML, Uitto J
J Clin Invest 1989 Jul;84(1):253-61. doi: 10.1172/JCI114148. PMID: 2500456 Free PMC Article

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