Welcome to OrphanAtlas

OrphanAtlas is your comprehensive resource for rare disease research, offering detailed insights into approximately 4000 rare diseases worldwide. Our platform provides access to both scientific and business information, empowering researchers, healthcare professionals, and policymakers.

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Prevalence
Lists the proportion of a population found affected by a certain medical condition at a specific time. It is typically indicated by the number of cases per 100,000 people
Geographic Spread
Shows the most affected age groups, genders, and regions for each condition, extracted using LLM-based queries from verified medical sources.
Publications
Provides the link to the number of publications for each listed medical condition over the last 5 years. These numbers are a reflection of the amount of research being done on these diseases
Classification
Lists each medical condition on the list as genetic vs non-genetic as well as one of 33 disease classifications as given on the Orphanet website
Symptoms
Describes the common and distinguishing signs, symptoms, and clinical presentations associated with each listed medical condition, helping in early identification and diagnosis.
Inheritance
Transfer of genetic information from parents to offsprings that may lead to the child inheriting a genetic disease or condition
Approved Treatments
Names of approved treatments, as taken from the FDA list of approved orphan drugs, where available, for the listed medical conditions
Pipeline Drugs
Drugs under development, where available, for the listed medical conditions
Genetic Variation
Gives the type of genetic variation and details of the genes affected, where available
AI Insights
Uses AI and Large Language Models (LLMs) to enrich data by extracting updated insights from verified medical sources, providing users with contextual and real-time information.

Database Categories

Prevalence
Lists the proportion of a population found affected by a certain medical condition at a specific time. It is typically indicated by the number of cases per 100,000 people
Publications
Provides the link to the number of publications for each listed medical condition over the last 5 years. These numbers are a reflection of the amount of research being done on these diseases
Classification
Lists each medical condition on the list as genetic vs non-genetic as well as one of 33 disease classifications as given on the Orphanet website
Inheritance
Transfer of genetic information from parents to offsprings that may lead to the child inheriting a genetic disease or condition
Approved Treatments
Names of approved treatments, as taken from the FDA list of approved orphan drugs, where available, for the listed medical conditions
Pipeline Drugs
Drugs under development, where available, for the listed medical conditions
Genetic Variation
Gives the type of genetic variation and details of the genes affected, where available
AI Insights
Uses AI and Large Language Models (LLMs) to enrich data by extracting updated insights from verified medical sources, providing users with contextual and real-time information.
Demographic Spread
Shows the most affected age groups, genders, and regions for each condition, extracted using LLM-based queries from verified medical sources.