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Complete mapping of diseases to ICD-10 codes with hierarchical navigation and cross-references
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Interconnected medical data showing relationships between diseases, symptoms, and treatments
Featured Medical Conditions
Nuclear type mitochondrial complex i deficiency 24
Mitochondrial Complex I Deficiency Nuclear Type 24 Mitochondrial complex I deficiency nuclear type 24 (MC1DN24) is a rare genetic disorder that affec...
Juvenile xanthogranuloma
What is Juvenile Xanthogranuloma? Juvenile xanthogranuloma (JXG) is a rare benign histiocytic proliferation that develops in infants and young childr...
Usher syndrome type 2d
Usher Syndrome Type 2D: A Rare Genetic Disorder Usher syndrome type 2D is a rare genetic disorder characterized by congenital, bilateral sensorineura...
Syndromic x-linked intellectual disability cabezas type
The Cabezas type of X-linked syndromic intellectual developmental disorder is characterized primarily by short stature, hypogonadism, and abnormal gai...
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Last Updated: 11/24/2024