ID   HPS2378
AC   CVCL_A3RB
DR   RCB; HPS2378
DR   Wikidata; Q105508650
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2378).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_UP11 ! HPS2377
OI   CVCL_A3RC ! HPS2379
OI   CVCL_A3RD ! HPS2380
OI   CVCL_A3RE ! HPS2381
OI   CVCL_A3RF ! HPS2382
SX   Male
AG   70-79Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 19-12-24; Version: 6
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