Rare Disease Reference (Orphanet). Rare disease reference from Orphanet by name or ORPHAcode: definition, synonyms, ICD-10 / ICD-11 / OMIM / UMLS / MeSH codes, inheritance, age of onset, prevalence estimates, and clinical features (HPO phenotypes) ranked by frequency with diagnostic-criterion flags. Orphadata, CC BY 4.0; not medical advice.
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