disease 904 words KG: ent-dise-30676b1b
Contents

Huntington Disease-Like 1 (HDL1)

Disease Info
InheritanceAutosomal dominant
GenePRNP (Prion Protein Gene)
Chromosome20p13
MutationOctapeptide repeat insertion (7-9 repeats)
ProteinAbnormal prion protein (PrP<sup>Sc</sup>)
DatabasesOMIMOrphanetClinicalTrialsPubMed

No AI portrait yet

Knowledge Graph

Community Feedback

0 0 upvotes · 0 downvotes
💬 0 comments ⚠ 0 flags ✏ 0 edit suggestions

No comments yet. Be the first to comment!

View all feedback (JSON)