Additional Disease Briefs

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Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
eosinophilic fasciitis

Also known as: EF, Shulman syndrome, diffuse fasciitis with eosinophilia, eosinophilic fasciitis, eosinophilic fasciitis (disease)

eosinophilic granuloma

Also known as: Monostotic Langerhans cell histiocytosis, chronic and localised Langerhans cell histiocytosis, chronic and localized Langerhans cell histiocytosis, chronic unifocal Langerhans cell histiocytosis, eosinophilic granuloma, eosinophilic xanthomatous granuloma, unifocal Langerhans cell histiocytosis

ependymal tumor of brain

Also known as: brain ependymal tumor, brain ependymal tumour, brain ependymoma, ependymal tumor of brain, ependymoma of brain

ependymoblastoma

Also known as: ETANTR, ETMR, ETMR, C19MC-altered, embryonal tumor with Multilayered Rosettes, embryonal tumor with Multilayered Rosettes with C19MC amplification, embryonal tumor with Multilayered Rosettes, C19MC-altered, embryonal tumor with abundant neuropil and true Rosettes, embryonal tumor with abundant neuropil and true rosettes, embryonal tumour with Multilayered Rosettes, embryonal tumour with Multilayered Rosettes with C19MC amplification, embryonal tumour with Multilayered Rosettes, C19MC-altered, embryonal tumour with abundant neuropil and true Rosettes, embryonal tumour with abundant neuropil and true rosettes, ependymoblastoma, neuroectodermal tumors primitive, neuroectodermal tumours primitive

ependymoma

Also known as: WHO grade II ependymal neoplasm, WHO grade II ependymal tumor, WHO grade II ependymal tumour, benign ependymoma, clear cell ependymoma (histologic variant), ependymoma, ependymoma, benign, ependymoma, familial, epithelial ependymoma, papillary ependymoma (histologic variant), tanycytic ependymoma (histologic variant)

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