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Hunter-Carpenter-MacDonald Syndrome


  • […] syndrome ORPHA:2174 Synonym(s): - Prevalence: - Inheritance: - Age of onset: - ICD-10: - OMIM: - UMLS: - MeSH: - GARD: 2751 MedDRA: - Summary This disease has been moved to Infantile neuroaxonal dystrophy The documents contained in this web site are presented[orpha.net]
  • In-Depth Information The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers.[rarediseases.info.nih.gov]


  • The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.[orpha.net]

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