Rare diseases

ORPHA nomenclature

The ORPHA nomenclature of each rare disease, with Orphanet data.

Real capture from the appAlexander disease sheet with ORPHA 58 code, ICD-10, prevalence, age of onset and inheritance (Orphadata)

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Licence CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). Reorganised and drawn as charts by Anasalva; texts may be translated.

What it does

Shows the ORPHA code, name and synonyms of each disease.

For professionals, students, patients and families looking for reliable information on a rare disease. It does not replace specialist care.

A section of the disease sheet, with its source cited.

The information in the app guides you and does not replace professional judgement.

Functional consequences
The functional consequences of each rare disease, with Orphanet data.
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Associated phenotypes
The associated phenotypes of each rare disease, with Orphanet data.
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Epidemiological data
The epidemiological data of each rare disease, with Orphanet data.
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Nosological definition
The nosological definition of each rare disease, with Orphanet data.
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Natural history
The natural history of each rare disease, with Orphanet data.
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Rare diseases
Rare disease sheets with Orphanet data.