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MIM:143100 - HUNTINGTON DISEASE; HD
Xenbase Genes: htt
Human Disease Resource: OMIM
MONDO:0007739 - Huntington disease |
MONDO:0016621 - juvenile Huntington disease |
DOID:12858 - Huntington's disease |
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MONDO:0007739 - Huntington disease |
MONDO:0016621 - juvenile Huntington disease |
DOID:12858 - Huntington's disease |